6a29bc1077e1bd2926fa1508c6fdde383397f4a4
mspeir
  Tue Sep 8 16:14:56 2026 -0700
relatedTracks.ra: drop 20 entries naming tracks that are not on the RR

An audit of the table against the public trackDb found 77 relationship rows
pointing at a track the RR does not have. Most are fine and stay: the track is
either gated behind an alpha include and still in development (LCRs, gerp,
imprinting, mei, srSv, t2tChain, tads, TOGAv2, clinvarMapped, colorsDbLegacy,
hg38Patch11, singleCellSignalsPeaks, cancerMutations), or the family is already
public on other assemblies and only this version or assembly has yet to be
pushed (transMapV6, crispr10K, tanDups, ukbDepletion). Those entries start
working on their own when the track ships.

The 20 lines removed here name tracks with no public counterpart under any name
on any assembly, so they could never render for a reader on the RR:

ucscRetroAli8, superseded by the V9 track that is public
wgRnaOld and cancerMutations, both release alpha
transMapV4, absent from the RR entirely, so the source page does not exist
ensGene on hg38 and mm10, where Ensembl Genes was retired
sibAltEvents, public on no assembly
chainNetHs1, which is assembly-hub machinery rather than a native hg38 track
cloneEndUcsc, a mapping that only ever existed on hgwdev

The three crispr lines came out for a different reason. On hgwdev crispr is a
superTrack over crisprRanges and crisprTargets while the RR carries only the
standalone crisprAllTargets, so the entries looked like they wanted repointing.
The file already relates crisprAllTargets and crispr10K reciprocally further
down, on all three assemblies, which made them redundant instead.

Every name still in the file resolves in the hgwdev trackDb, and no duplicate
assembly and track pair remains. Rebuilt with make update on hg38, hg19 and
mm10: 24 rows dropped, none added, nothing else changed.

The original audit checked names against alpha, which is why these got in.

refs #38016

Co-Authored-By: Claude Opus 5 (1M context) <noreply@anthropic.com>

diff --git src/hg/makeDb/trackDb/relatedTracks.ra src/hg/makeDb/trackDb/relatedTracks.ra
index 97cea089e65..62c7ece2f1f 100644
--- src/hg/makeDb/trackDb/relatedTracks.ra
+++ src/hg/makeDb/trackDb/relatedTracks.ra
@@ -1,632 +1,612 @@
 # A space delimited file of track relatedness. Format:
 # ucscDb track trackLinkingTo reason
 #
 # By default entries are reciprocal, so each relationship needs a line in each
 # direction. Prefix the first track with '>' for a relationship that only goes one
 # way, or with '~' to get both directions out of a single line when the reason is
 # the same either way. Neither form needs a reciprocal line. Format:
 # ucscDb >track trackLinkingTo reason
 # ucscDb ~track trackLinkingTo reason
 #
 # The reason is displayed after the linked track's short label, as
 # "Short Label: reason", so do not begin the reason with the track's own name.
 
 # hg38:
 hg38 knownGene knownGeneArchive View previous versions of GENCODE Genes
 hg38 knownGeneArchive knownGene View the latest GENCODE Genes version
 
 hg38 miRnaAtlas nonCodingRNAs View associated precursor miRnas
 hg38 nonCodingRNAs miRnaAtlas View expression of cleaved miRnas
 
 hg38 caddSuper gnomadVariants View associated variants
 hg38 gnomadVariants caddSuper View CADD scores for this variant and region
 
 hg38 constraintSuper gnomadPLI Predicted constraint metrics from gnomAD
 hg38 gnomadPLI constraintSuper Container track of various constraint scores
 
 hg38 >imprinting humanMethylationAtlasSummary Methylation of purified cell types, from the Kaplan lab
 hg38 >humanMethylationAtlasSummary imprinting Imprinted genes and allele-specific methylation
 
 hg38 gnomadStr strVar Population-level short tandem repeat and VNTR variation from multiple projects
 hg38 strVar gnomadStr Short tandem repeat genotypes at disease-associated loci, from gnomAD v3.1.3
 
 hg38 varFreqs gnomadVariants Harmonized allele frequencies from ~800,000 exomes and genomes
 hg38 gnomadVariants varFreqs Allele frequencies from population-scale projects worldwide, not reprocessed by gnomAD
 
 hg38 varFreqs strVar Population-level short tandem repeat and VNTR variation from multiple projects
 hg38 strVar varFreqs SNV and indel allele frequencies from population-scale sequencing and array projects
 
 hg38 >revel liftHg19 REVEL is based on hg19 and lifted to hg38 with these liftOver chain alignments
 
 hg38 revel caddSuper A similar deleteriousness score, not used as an input by REVEL
 hg38 caddSuper revel A similar deleteriousness score
 
 hg38 liftHg19 grcIncidentDb Reasons why the assembly was changed in this region
 hg38 grcIncidentDb liftHg19 Explore how incident regions aligned between the human assemblies
 
 hg38 ReMap liftHg19 NCBI ReMap, even though it has the same name, is a liftOver-like hg19/hg38 alignment, and unrelated to the ReMap database
 hg38 liftHg19 ReMap Even though it has the same name, this is a database of transcription factor binding sites, unrelated to NCBI ReMap
 
 hg38 ReMap jaspar A database of predicted TF binding sites, based on short DNA matches. Unlike ReMap, the data is purely computational.
 
 hg38 jaspar ReMap A database of TF binding sites inferred from ChIP-Seq data. Unlike JASPAR predictions, these sites are supported by functional assay
 
 hg38 problematic mappability Regions where short sequencing reads are hard to align
 hg38 mappability problematic Various gene clusters and the ENCODE blacklist
 hg38 problematic grcIncidentDb Regions flagged by the Genome Reference Consortium, the group that puts together the genome
 hg38 grcIncidentDb problematic Unusual regions, and the ones that often lead to artefacts when aligning reads to the reference genome
 
 hg38 phasedVars varFreqs Projects where variant frequencies, aka allele frequencies, are publicly available
 hg38 varFreqs phasedVars Projects that provide haplotype-phased genotypes and variants
 
 hg38 wgEncodeReg4 wgEncodeReg The previous version of this track
 hg38 wgEncodeReg wgEncodeReg4 The newer version of this track
 hg38 ~wgEncodeReg4 cCREs Related ENCODE4 data
 
 hg38 >avada varaico The latest variants mined from published papers. The AVADA track is no longer updated.
 
 # hg19:
 hg19 caddSuper gnomadSuper View associated variants
 hg19 gnomadSuper caddSuper View CADD scores for this variant and region
 
 hg19 decipherHaploIns gnomadPLI Compare haploinsufficiency metrics as defined by gnomAD
 hg19 gnomadPLI decipherHaploIns Compare constraint metrics as defined by DECIPHER
 
 hg19 revel caddSuper A similar deleteriousness score, not used as an input by REVEL
 hg19 caddSuper revel A similar deleteriousness score
 
 hg19 liftHg38 grcIncidentDb Reasons why the assembly was changed in this region
 hg19 grcIncidentDb liftHg38 Alignments between hg19 and hg38, to explore how GRC incident assembly changes affect the whole-genome alignments used for lifting data from hg19
 
 hg19 fixSeqLiftOverPsl liftHg38 Investigate how patches affect the whole-genome alignment used for liftOver
 hg19 liftHg38 fixSeqLiftOverPsl Investigate how assembly patches affect the liftOver alignment
 
 hg19 liftHg38 hg38ContigDiff Contigs that were changed from hg19 to hg38
 hg19 hg38ContigDiff liftHg38 Investigate how contig changes affect the liftOver alignments
 
 hg19 jaspar ReMap A database of TF binding sites inferred from ChIP-Seq data. Unlike JASPAR predictions, these sites are supported by functional assay
 hg19 ReMap jaspar A database of predicted TF binding sites, based on short DNA matches. Unlike ReMap, the data is purely computational.
 
 hg19 ReMap liftHg38 NCBI ReMap, even though it has the same name, is a liftOver-like hg19/hg38 alignment, and unrelated to the ReMap database
 hg19 liftHg38 ReMap Even though it has the same name, this is a database of transcription factor binding sites, unrelated to NCBI ReMap
 
 hg19 >pseudoYale60 refSeqComposite The Curated and Other subtracks also contain some transcribed and untranscribed pseudogenes, respectively
 
 hg19 constraintSuper gnomadPLI Predicted constraint metrics from gnomAD
 hg19 gnomadPLI constraintSuper Container track of various constraint scores
 
 hg19 >avada varaico The latest variants mined from published papers. The AVADA track is no longer updated.
 
 # mm39:
 
 mm39 knownGene knownGeneArchive View previous versions of GENCODE Genes
 mm39 knownGeneArchive knownGene View the latest GENCODE Genes version
 
 # mm10 ENCODE4 Regulation:
 mm10 encode4Reg encode3Reg The previous version of this track
 mm10 encode3Reg encode4Reg The newer version of this track
 mm10 ~encode4Reg cCREs Related ENCODE4 data
 mm10 ~mouseDevTimecourse encode3Reg Related ENCODE track
 mm10 ~mouseDevTimecourse encode4Reg Related ENCODE track
 
 # mm10 mouse gene expression cross-links:
 mm10 mouseDevTimecourse tabulaMuris Single-cell gene expression across adult mouse organs
 mm10 tabulaMuris mouseDevTimecourse Bulk RNA-seq gene expression across mouse development
 
 # hg38 long-read SV supertrack cross-links to other SV resources:
 hg38 longReadVariants gnomadStructuralVariants Short-read structural variants from gnomAD v4.1
 hg38 gnomadStructuralVariants longReadVariants Long-read structural variants across multiple cohorts
 hg38 longReadVariants dbVarSv NCBI dbVar structural variants (short-read and long-read, germline and clinical)
 hg38 dbVarSv longReadVariants Long-read structural variants across multiple cohorts
 hg38 longReadVariants dgvPlus Database of Genomic Variants (DGV) structural variation catalog
 hg38 dgvPlus longReadVariants Long-read structural variants across multiple cohorts
 hg38 longReadVariants giabSv Genome in a Bottle high-confidence SV benchmark callsets
 hg38 giabSv longReadVariants Long-read structural variants across multiple cohorts
 hg38 longReadVariants mei Polymorphic Mobile Element Insertions (Alu, L1, SVA, HERVK, snRNA) from HGSVC3 long-read assemblies
 hg38 mei longReadVariants Long-read structural variants across multiple cohorts (parent SV callsets for the HGSVC3 MEI track)
 hs1 longReadVariants mei Polymorphic Mobile Element Insertions (Alu, L1, SVA, HERVK, snRNA) from HGSVC3 long-read assemblies
 hs1 mei longReadVariants Long-read structural variants across multiple cohorts (parent SV callsets for the HGSVC3 MEI track)
 
 # EVE cross-links:
 hg38 eve alphaMissense A similar deep-learning missense pathogenicity predictor
 hg38 alphaMissense eve A missense pathogenicity predictor trained on evolutionary sequence variation
 hg38 eve primateAi A similar deep-learning missense pathogenicity predictor using primate variation
 hg38 primateAi eve A missense pathogenicity predictor trained on evolutionary sequence variation
 hg38 eve revel An ensemble missense pathogenicity score built from multiple predictors
 hg38 revel eve A missense pathogenicity predictor trained on evolutionary sequence variation
 hg38 eve clinPred An ensemble missense pathogenicity predictor that incorporates gnomAD allele frequency
 hg38 clinPred eve A missense pathogenicity predictor trained on evolutionary sequence variation
 
 # PrimateAI-3D cross-links:
 hg38 ~primateAi alphaMissense A similar deep-learning missense pathogenicity predictor
 hg38 primateAi revel An ensemble missense pathogenicity score built from multiple predictors
 hg38 revel primateAi A missense pathogenicity predictor using primate variation and 3D protein structure
 
 hg19 primateAi revel An ensemble missense pathogenicity score built from multiple predictors
 hg19 revel primateAi A missense pathogenicity predictor using primate variation and 3D protein structure
 
 # ClinPred cross-links:
 hg38 clinPred revel An ensemble missense pathogenicity score using a similar machine-learning approach
 hg38 revel clinPred An ensemble missense pathogenicity predictor that incorporates gnomAD allele frequency
 hg38 clinPred caddSuper A similar deleteriousness score
 hg38 caddSuper clinPred A missense-only pathogenicity predictor
 hg38 clinPred primateAi A missense pathogenicity predictor using primate variation
 hg38 primateAi clinPred An ensemble missense predictor incorporating gnomAD allele frequency
 hg38 clinPred alphaMissense A deep-learning missense pathogenicity predictor
 hg38 alphaMissense clinPred An ensemble missense predictor incorporating gnomAD allele frequency
 
 # popEVE cross-links:
 hg38 popEve eve A missense pathogenicity predictor trained on evolutionary sequence variation, and an input to popEVE
 hg38 eve popEve A proteome-wide missense deleteriousness model built on EVE and calibrated with human population data
 hg38 popEve alphaMissense A similar deep-learning missense pathogenicity predictor
 hg38 alphaMissense popEve A proteome-wide missense deleteriousness model combining evolutionary and human population data
 hg38 popEve primateAi A similar deep-learning missense pathogenicity predictor using primate variation
 hg38 primateAi popEve A proteome-wide missense deleteriousness model combining evolutionary and human population data
 hg38 popEve clinPred An ensemble missense pathogenicity predictor that incorporates gnomAD allele frequency
 hg38 clinPred popEve A proteome-wide missense deleteriousness model combining evolutionary and human population data
 hg38 popEve revel An ensemble missense pathogenicity score built from multiple predictors
 hg38 revel popEve A proteome-wide missense deleteriousness model combining evolutionary and human population data
 
 hg19 clinPred revel An ensemble missense pathogenicity score using a similar machine-learning approach
 hg19 revel clinPred An ensemble missense pathogenicity predictor that incorporates gnomAD allele frequency
 hg19 clinPred caddSuper A similar deleteriousness score
 hg19 caddSuper clinPred A missense-only pathogenicity predictor
 hg19 clinPred primateAi A missense pathogenicity predictor using primate variation
 hg19 primateAi clinPred An ensemble missense predictor incorporating gnomAD allele frequency
 hg19 clinPred alphaMissense A deep-learning missense pathogenicity predictor
 hg19 alphaMissense clinPred An ensemble missense predictor incorporating gnomAD allele frequency
 
 # PromoterAI cross-links:
 hg38 promoterAi primateAi A companion deep-learning model from Illumina for coding (missense) variants
 hg38 primateAi promoterAi A companion deep-learning model from Illumina for non-coding promoter variants
 hg38 promoterAi alphaMissense A deep-learning predictor of missense (coding) variant pathogenicity
 hg38 alphaMissense promoterAi A deep-learning predictor of expression-altering variants in promoter regions
 
 # NMD Escape cross-links:
 hg38 >nmd mane Select transcripts from NCBI and EBI, a curated subset of RefSeq and Ensembl transcripts used as a clinical reference
 hg38 >nmd ncbiRefSeq NCBI RefSeq transcripts, the source annotation set for the NMD Escape RefSeq subtrack
 
 # MPRA cross-links:
 hg38 mpra wgEncodeReg4 ENCODE regulatory region annotations, many of which are tested by MPRA assays
 hg38 wgEncodeReg4 mpra Experimental MPRA measurements of regulatory activity for candidate elements
 hg38 mpra cCREs Candidate cis-regulatory elements; many overlap MPRA-tested fragments
 hg38 cCREs mpra Experimentally validated regulatory activity from MPRA assays for overlapping elements
 
 # Dosage sensitivity / CNV cross-links:
 hg38 clinGenComp dosageSensitivity Predicted gene-level haploinsufficiency (pHaplo) and triplosensitivity (pTriplo) scores from Collins et al. 2022, complementary to ClinGen's expert-curated dosage sensitivity calls
 hg38 dosageSensitivity clinGenComp ClinGen expert-curated dosage sensitivity (haploinsufficiency and triplosensitivity) and gene-disease validity assertions
 hg38 clinGenComp cnvDevDelay Copy Number Variation Morbidity Map of Developmental Delay: case/control CNV regions associated with developmental delay phenotypes
 hg38 cnvDevDelay clinGenComp ClinGen expert-curated dosage sensitivity and gene-disease validity assertions for genes within CNV regions
 hg38 dosageSensitivity cnvDevDelay Copy Number Variation Morbidity Map of Developmental Delay: case/control CNV regions providing phenotypic context for dosage-sensitive genes
 hg38 cnvDevDelay dosageSensitivity Predicted gene-level haploinsufficiency (pHaplo) and triplosensitivity (pTriplo) scores from Collins et al. 2022 for genes within these CNVs
 
 hg19 clinGenComp dosageSensitivity Predicted gene-level haploinsufficiency (pHaplo) and triplosensitivity (pTriplo) scores from Collins et al. 2022, complementary to ClinGen's expert-curated dosage sensitivity calls
 hg19 dosageSensitivity clinGenComp ClinGen expert-curated dosage sensitivity (haploinsufficiency and triplosensitivity) and gene-disease validity assertions
 hg19 clinGenComp cnvDevDelay Copy Number Variation Morbidity Map of Developmental Delay: case/control CNV regions associated with developmental delay phenotypes
 hg19 cnvDevDelay clinGenComp ClinGen expert-curated dosage sensitivity and gene-disease validity assertions for genes within CNV regions
 hg19 dosageSensitivity cnvDevDelay Copy Number Variation Morbidity Map of Developmental Delay: case/control CNV regions providing phenotypic context for dosage-sensitive genes
 hg19 cnvDevDelay dosageSensitivity Predicted gene-level haploinsufficiency (pHaplo) and triplosensitivity (pTriplo) scores from Collins et al. 2022 for genes within these CNVs
 
 # danRer11 BAC clone tracks:
 danRer11 bacEndPairsLift choriCloneEnds CHORI zebrafish BAC clone end placements (CH73, CH211, CH1073) from NCBI Clone DB on GRCz11
 danRer11 choriCloneEnds bacEndPairsLift Zebrafish BAC end pairs lifted from danRer4 (older UCSC BLAT placements)
 
 # Relationships added from the #38016 audit. Version successions run one way,
 # from the older track to the newer one; archives are reciprocal.
 
 # Version successions, from the older track to the newer one:
 hg38 >caddSuper caddSuper1_7 The newer CADD release, with an updated model and training set
 hg38 >cosmicRegions cosmicMuts Individual somatic mutations from the current COSMIC release (V101)
 hg38 dbSnp155Composite dbSnpArchive Older dbSNP builds, kept for reproducing earlier analyses
 hg38 dbSnpArchive dbSnp155Composite The dbSNP release currently used by the Browser
 hg38 >gtexGene gtexGeneV8 The newer GTEx release, 54 tissues from 948 donors
-hg38 >ucscRetroAli8 ucscRetroAli9 The newer version of this track
-hg38 >wgRnaOld wgRna The newer version of this track
 hg38 >covidHgiGwas covidHgiGwasR4Pval A later release of the same COVID-19 Host Genetics Initiative meta-analysis
 hg38 >colorsDbLegacy longReadVariants Current long-read structural variant callsets, including the up-to-date CoLoRSdb release
-hg38 >crispr crispr10K The same target sites computed over a wider window, exons plus 10 kb rather than 200 bp
-hg38 >transMapV4 transMapV6 The current version of the TransMap alignments
 hg38 >transMapV5 transMapV6 The current version of the TransMap alignments
 hg38 knownGeneArchive wgEncodeGencodeSuper All transcripts from each GENCODE release, including sets never used as the default gene track
 hg38 wgEncodeGencodeSuper knownGeneArchive Previous default gene tracks, one per GENCODE release
 hg38 >genePredArchive knownGene The current default gene set
-hg38 >ensGene knownGene The current GENCODE gene set, which shares its annotation with Ensembl
 
 hg19 >caddSuper caddSuper1_7 The newer CADD release, with an updated model and training set
 hg19 >cosmicRegions cosmicMuts Individual somatic mutations from the current COSMIC release (V101)
 hg19 dbSnp155Composite dbSnpArchive Older dbSNP builds, kept for reproducing earlier analyses
 hg19 dbSnpArchive dbSnp155Composite The dbSNP release currently used by the Browser
 hg19 >gtexGene gtexGeneV8 The newer GTEx release, 54 tissues from 948 donors
-hg19 >wgRnaOld wgRna The newer version of this track
 hg19 >covidHgiGwas covidHgiGwasR4Pval A later release of the same COVID-19 Host Genetics Initiative meta-analysis
-hg19 >crispr crispr10K The same target sites computed over a wider window, exons plus 10 kb rather than 200 bp
-hg19 >transMapV4 transMapV6 The current version of the TransMap alignments
 hg19 >transMapV5 transMapV6 The current version of the TransMap alignments
 hg19 knownGeneArchive wgEncodeGencodeSuper All transcripts from each GENCODE release, including sets never used as the default gene track
 hg19 wgEncodeGencodeSuper knownGeneArchive Previous default gene tracks, one per GENCODE release
 hg19 >genePredArchive knownGene The current default gene set
-hg19 >ensGene knownGene The current GENCODE gene set, which shares its annotation with Ensembl
 
 mm39 knownGeneArchive wgEncodeGencodeSuper All transcripts from each GENCODE release, including sets never used as the default gene track
 mm39 wgEncodeGencodeSuper knownGeneArchive Previous default gene tracks, one per GENCODE release
 
-mm10 >crispr crispr10K The same target sites computed over a wider window, exons plus 10 kb rather than 200 bp
-mm10 >transMapV4 transMapV6 The current version of the TransMap alignments
 mm10 >transMapV5 transMapV6 The current version of the TransMap alignments
-mm10 >ensGene knownGene The current GENCODE gene set, which shares its annotation with Ensembl
 
 # Clinical variant database cross-links:
 hg38 clinvar hgmd Disease-causing mutations curated from the literature by HGMD; the public release lags the licensed version
 hg38 hgmd clinvar Variant interpretations submitted by clinical laboratories, with review status and conflicts
 hg38 clinvar lovdComp Variants collected in the gene-specific Leiden Open Variation Database instances
 hg38 lovdComp clinvar Variant interpretations submitted by clinical laboratories worldwide
 hg38 clinvar decipherContainer Patient variants and CNVs from the DECIPHER developmental disorder database
 hg38 decipherContainer clinvar Variant interpretations submitted by clinical laboratories, with review status
 hg38 clinvarMapped clinvar The original, directly submitted ClinVar variant records
 hg38 clinvar clinvarMapped Coding variants projected onto paralogous loci by sequence homology
 hg38 mitoMap nuMtSeq Mitochondrial segments inserted into the nuclear genome, a common source of false-positive chrM variant calls
 hg38 nuMtSeq mitoMap Variants and annotations on the mitochondrial genome itself
 
 hg19 clinvar hgmd Disease-causing mutations curated from the literature by HGMD; the public release lags the licensed version
 hg19 hgmd clinvar Variant interpretations submitted by clinical laboratories, with review status and conflicts
 hg19 clinvar lovdComp Variants collected in the gene-specific Leiden Open Variation Database instances
 hg19 lovdComp clinvar Variant interpretations submitted by clinical laboratories worldwide
 hg19 clinvar decipherContainer Patient variants and CNVs from the DECIPHER developmental disorder database
 hg19 decipherContainer clinvar Variant interpretations submitted by clinical laboratories, with review status
 
 # Gene-disease curation cross-links:
 hg38 genCC g2p Gene-disease pairs curated by the Gene2Phenotype project, one of the sources GenCC aggregates
 hg38 g2p genCC Gene-disease assertions from several curation groups, harmonized into one set
 hg38 genCC panelApp Diagnostic gene panels from Genomics England and Australia, one of the sources GenCC aggregates
 hg38 panelApp genCC Gene-disease assertions from several curation groups, harmonized into one set
 hg38 genCC orphadata Rare disease gene annotations from Orphanet, one of the sources GenCC aggregates
 hg38 orphadata genCC Gene-disease assertions from several curation groups, harmonized into one set
 hg38 genCC clinGenComp Expert-panel gene-disease validity and dosage sensitivity curation, one of the sources GenCC aggregates
 hg38 clinGenComp genCC Gene-disease assertions from several curation groups, harmonized into one set
 hg38 geneReviews omimContainer Gene and phenotype records from OMIM, the standard reference for Mendelian disease genes
 hg38 omimContainer geneReviews Expert-authored clinical summaries for genetic conditions, with diagnosis and management guidance
 hg38 genCC omimContainer Gene and phenotype records from OMIM, the reference these curation efforts cite
 hg38 omimContainer genCC Gene-disease assertions from several curation groups, harmonized into one set
 hg38 orphadata omimContainer Gene and phenotype records from OMIM, cross-referenced throughout Orphanet
 hg38 omimContainer orphadata Rare disease gene annotations from Orphanet
 hg38 g2p omimContainer Gene and phenotype records from OMIM, the reference these curation efforts cite
 hg38 omimContainer g2p Gene-disease pairs curated by the Gene2Phenotype project
 
 hg19 genCC g2p Gene-disease pairs curated by the Gene2Phenotype project, one of the sources GenCC aggregates
 hg19 g2p genCC Gene-disease assertions from several curation groups, harmonized into one set
 hg19 genCC panelApp Diagnostic gene panels from Genomics England and Australia, one of the sources GenCC aggregates
 hg19 panelApp genCC Gene-disease assertions from several curation groups, harmonized into one set
 hg19 genCC orphadata Rare disease gene annotations from Orphanet, one of the sources GenCC aggregates
 hg19 orphadata genCC Gene-disease assertions from several curation groups, harmonized into one set
 hg19 genCC clinGenComp Expert-panel gene-disease validity and dosage sensitivity curation, one of the sources GenCC aggregates
 hg19 clinGenComp genCC Gene-disease assertions from several curation groups, harmonized into one set
 hg19 geneReviews omimContainer Gene and phenotype records from OMIM, the standard reference for Mendelian disease genes
 hg19 omimContainer geneReviews Expert-authored clinical summaries for genetic conditions, with diagnosis and management guidance
 hg19 genCC omimContainer Gene and phenotype records from OMIM, the reference these curation efforts cite
 hg19 omimContainer genCC Gene-disease assertions from several curation groups, harmonized into one set
 hg19 orphadata omimContainer Gene and phenotype records from OMIM, cross-referenced throughout Orphanet
 hg19 omimContainer orphadata Rare disease gene annotations from Orphanet
 hg19 g2p omimContainer Gene and phenotype records from OMIM, the reference these curation efforts cite
 hg19 omimContainer g2p Gene-disease pairs curated by the Gene2Phenotype project
 
 # Cancer somatic variant cross-links:
 hg38 cancerMutations gdcCancer The same TCGA somatic mutations, summarized across all 33 Pan-Cancer projects
 hg38 gdcCancer cancerMutations TCGA somatic mutations shown separately for each cancer study
 hg38 cosmicMuts civic Clinically interpreted cancer variants, with evidence for diagnosis, prognosis and drug response
 hg38 civic cosmicMuts A broad catalog of somatic mutations reported in cancer, without clinical interpretation
 hg38 gdcCancer cancerExpr Gene expression measured in the same 33 TCGA cancer projects
 hg38 cancerExpr gdcCancer Somatic mutations called in the same 33 TCGA cancer projects
 hg38 >dbVar_somatic cosmicMuts A much larger catalog of somatic point mutations in cancer
 
 hg19 cosmicMuts civic Clinically interpreted cancer variants, with evidence for diagnosis, prognosis and drug response
 hg19 civic cosmicMuts A broad catalog of somatic mutations reported in cancer, without clinical interpretation
 hg19 >dbVar_somatic cosmicMuts A much larger catalog of somatic point mutations in cancer
 
 # Structural variation cross-links:
 hg38 >srSv longReadVariants The long-read structural variant callsets these short-read sets are compared against
 hg38 >platinumGenomes giab A larger and more current benchmark callset from well-characterized reference samples
 hg38 iscaComposite dgvPlus Structural variants seen in apparently healthy individuals, for frequency context
 hg38 dgvPlus iscaComposite Clinically curated CNVs from ClinGen, with pathogenicity assertions
 hg38 >coriellDelDup iscaComposite Clinically curated CNVs from ClinGen, with pathogenicity assertions
 hg38 iscaComposite clinGenComp Gene-level dosage sensitivity and gene-disease validity curation from the same expert panels
 hg38 clinGenComp iscaComposite Individual CNVs curated by ClinGen, with pathogenicity assertions
 hg38 ~genomicSuperDups tanDups Another view of near-identical duplicated sequence in the genome
 
 hg19 >platinumGenomes giab A larger and more current benchmark callset from well-characterized reference samples
 hg19 iscaComposite dgvPlus Structural variants seen in apparently healthy individuals, for frequency context
 hg19 dgvPlus iscaComposite Clinically curated CNVs from ClinGen, with pathogenicity assertions
 hg19 >coriellDelDup iscaComposite Clinically curated CNVs from ClinGen, with pathogenicity assertions
 hg19 iscaComposite clinGenComp Gene-level dosage sensitivity and gene-disease validity curation from the same expert panels
 hg19 clinGenComp iscaComposite Individual CNVs curated by ClinGen, with pathogenicity assertions
 hg19 ~genomicSuperDups tanDups Another view of near-identical duplicated sequence in the genome
 
 mm10 ~genomicSuperDups tanDups Another view of near-identical duplicated sequence in the genome
 
 # Tandem repeat cross-links:
 hg38 strVar simpleRepeat Tandem repeats annotated in the reference sequence by Tandem Repeats Finder
 hg38 simpleRepeat strVar Population variation in the length of tandem repeats
 hg38 ~trexplorer webstr Another genome-wide tandem repeat catalog with per-locus allele distributions
 hg38 ~microsat simpleRepeat Another annotation of short tandem repeats in the reference sequence
 
 hg19 ~microsat simpleRepeat Another annotation of short tandem repeats in the reference sequence
 
 mm39 ~microsat simpleRepeat Another annotation of short tandem repeats in the reference sequence
 
 mm10 ~microsat simpleRepeat Another annotation of short tandem repeats in the reference sequence
 
 # Allele frequency cross-links:
 hg38 >tgpArchive varFreqs Allele frequencies from many newer population-scale sequencing projects
 
 # Regulation cross-links:
 hg38 geneHancer oreganno Literature-curated regulatory elements and transcription factor binding sites
 hg38 oreganno geneHancer Enhancers and promoters with predicted target genes, integrated from several sources
 hg38 geneHancer vistaEnhancersBb Enhancers tested for activity in transgenic mouse embryos
 hg38 vistaEnhancersBb geneHancer Predicted enhancers and promoters with their likely target genes
 hg38 cCREs refSeqFuncElems Regulatory and other functional elements curated by NCBI from the literature
 hg38 refSeqFuncElems cCREs Candidate regulatory elements called from ENCODE chromatin data
 hg38 tads hicAndMicroC The Hi-C and Micro-C contact maps that domain boundaries are called from
 hg38 hicAndMicroC tads Topologically associating domains and boundaries called from contact maps
 hg38 cpgIslandSuper dnaMethylation Measured methylation levels, which are often depleted over these islands
 hg38 dnaMethylation cpgIslandSuper CpG-dense regions predicted from the reference sequence
 hg38 epdNew fantom5 Transcription start sites and their usage, measured by CAGE
 hg38 fantom5 epdNew Experimentally supported promoters curated in EPDnew
 hg38 gtexEqtlHighConf gtexGeneV8 Gene expression levels in the same GTEx tissues
 hg38 gtexGeneV8 gtexEqtlHighConf Variants associated with expression of nearby genes in the same tissues
 hg38 jaspar wgEncodeReg4TfPeaks Transcription factor peak clusters from ENCODE 4 ChIP-seq experiments
 hg38 wgEncodeReg4TfPeaks jaspar Computationally predicted binding sites from position weight matrices
 hg38 singleCellSignalsPeaks wgEncodeReg4Atac Bulk ATAC-seq accessibility, averaged by organ and tissue
 hg38 wgEncodeReg4Atac singleCellSignalsPeaks Chromatin accessibility resolved by individual cell type
 
 hg19 geneHancer oreganno Literature-curated regulatory elements and transcription factor binding sites
 hg19 oreganno geneHancer Enhancers and promoters with predicted target genes, integrated from several sources
 hg19 geneHancer vistaEnhancersBb Enhancers tested for activity in transgenic mouse embryos
 hg19 vistaEnhancersBb geneHancer Predicted enhancers and promoters with their likely target genes
 hg19 cpgIslandSuper dnaMethylation Measured methylation levels, which are often depleted over these islands
 hg19 dnaMethylation cpgIslandSuper CpG-dense regions predicted from the reference sequence
 hg19 epdNew fantom5 Transcription start sites and their usage, measured by CAGE
 hg19 fantom5 epdNew Experimentally supported promoters curated in EPDnew
 
 mm39 cpgIslandSuper dnaMethylation Measured methylation levels, which are often depleted over these islands
 mm39 dnaMethylation cpgIslandSuper CpG-dense regions predicted from the reference sequence
 
 mm10 cCREs refSeqFuncElems Regulatory and other functional elements curated by NCBI from the literature
 mm10 refSeqFuncElems cCREs Candidate regulatory elements called from ENCODE chromatin data
 
 danRer11 cpgIslandSuper dnaMethylation Measured methylation levels, which are often depleted over these islands
 danRer11 dnaMethylation cpgIslandSuper CpG-dense regions predicted from the reference sequence
 
 # Gene and protein cross-links:
 hg38 uniprot spMut Amino acid substitutions annotated in UniProt, mapped to the genome
 hg38 spMut uniprot Protein domains, sites and other UniProt annotations mapped to the genome
 hg38 ucscGenePfam uniprot Protein domains and functional sites from UniProt
 hg38 uniprot ucscGenePfam Pfam domains mapped onto GENCODE transcripts
 hg38 knownGene mane One representative transcript per gene, agreed between RefSeq and GENCODE
 hg38 mane knownGene The full GENCODE gene set that MANE Select transcripts are drawn from
 hg38 refSeqComposite mane The MANE Select subset of RefSeq transcripts, matched to GENCODE
 hg38 mane refSeqComposite The full NCBI RefSeq transcript set that MANE Select is drawn from
 hg38 knownGene hgnc Official gene symbols and names from the HGNC, with previous symbols and aliases
 hg38 hgnc knownGene The default gene set, whose gene names come from this nomenclature
 hg38 refSeqComposite hgnc Official gene symbols and names from the HGNC, with previous symbols and aliases
 hg38 hgnc refSeqComposite Transcript annotations from NCBI, which use these gene symbols
 hg38 mane hgnc Official gene symbols and names from the HGNC, with previous symbols and aliases
 hg38 hgnc mane One agreed representative transcript per gene, matched between RefSeq and GENCODE
 hg38 >ccdsGene mane One representative transcript per gene, matched between RefSeq and GENCODE
 hg38 refSeqComposite xenoRefGene RefSeq transcripts from other species, aligned to the human genome
 hg38 xenoRefGene refSeqComposite Human RefSeq transcripts, rather than transcripts from other species
-hg38 ~knownAlt sibAltEvents Another set of alternative splicing and promoter events called from transcript alignments
-hg38 sibTxGraph sibAltEvents Individual alternative splicing and polyadenylation events derived from this graph
-hg38 sibAltEvents sibTxGraph The full alternative splicing graph these events are derived from
 hg38 pseudogenes ucscRetroAli9 Retroposed gene copies, a major source of processed pseudogenes
 hg38 ucscRetroAli9 pseudogenes Curated pseudogene annotations from GENCODE and Yale
 hg38 ncOrfs gwipsvizRiboseq Ribosome profiling data, the main evidence for translation of non-canonical ORFs
 hg38 gwipsvizRiboseq ncOrfs Open reading frames outside annotated CDS regions, called partly from ribosome profiling
 hg38 lrg lrgTranscriptAli The fixed LRG transcript annotations within these regions
 hg38 lrgTranscriptAli lrg The genomic LRG reference regions these transcripts belong to
 hg38 crispr10K crisprAllTargets Cas9 target sites across the whole genome, not only near exons
 hg38 crisprAllTargets crispr10K Cas9 target sites restricted to exons and 10 kb of flanking sequence
 
 hg19 uniprot spMut Amino acid substitutions annotated in UniProt, mapped to the genome
 hg19 spMut uniprot Protein domains, sites and other UniProt annotations mapped to the genome
 hg19 ucscGenePfam uniprot Protein domains and functional sites from UniProt
 hg19 uniprot ucscGenePfam Pfam domains mapped onto GENCODE transcripts
 hg19 knownGene hgnc Official gene symbols and names from the HGNC, with previous symbols and aliases
 hg19 hgnc knownGene The default gene set, whose gene names come from this nomenclature
 hg19 refSeqComposite hgnc Official gene symbols and names from the HGNC, with previous symbols and aliases
 hg19 hgnc refSeqComposite Transcript annotations from NCBI, which use these gene symbols
 hg19 refSeqComposite xenoRefGene RefSeq transcripts from other species, aligned to the human genome
 hg19 xenoRefGene refSeqComposite Human RefSeq transcripts, rather than transcripts from other species
-hg19 ~knownAlt sibAltEvents Another set of alternative splicing and promoter events called from transcript alignments
-hg19 sibTxGraph sibAltEvents Individual alternative splicing and polyadenylation events derived from this graph
-hg19 sibAltEvents sibTxGraph The full alternative splicing graph these events are derived from
 hg19 lrg lrgTranscriptAli The fixed LRG transcript annotations within these regions
 hg19 lrgTranscriptAli lrg The genomic LRG reference regions these transcripts belong to
 hg19 crispr10K crisprAllTargets Cas9 target sites across the whole genome, not only near exons
 hg19 crisprAllTargets crispr10K Cas9 target sites restricted to exons and 10 kb of flanking sequence
 
 mm39 ucscGenePfam uniprot Protein domains and functional sites from UniProt
 mm39 uniprot ucscGenePfam Pfam domains mapped onto GENCODE transcripts
 mm39 refSeqComposite xenoRefGene RefSeq transcripts from other species, aligned to the human genome
 mm39 xenoRefGene refSeqComposite Human RefSeq transcripts, rather than transcripts from other species
 
 mm10 uniprot spMut Amino acid substitutions annotated in UniProt, mapped to the genome
 mm10 spMut uniprot Protein domains, sites and other UniProt annotations mapped to the genome
 mm10 ucscGenePfam uniprot Protein domains and functional sites from UniProt
 mm10 uniprot ucscGenePfam Pfam domains mapped onto GENCODE transcripts
 mm10 refSeqComposite xenoRefGene RefSeq transcripts from other species, aligned to the human genome
 mm10 xenoRefGene refSeqComposite Human RefSeq transcripts, rather than transcripts from other species
 mm10 crispr10K crisprAllTargets Cas9 target sites across the whole genome, not only near exons
 mm10 crisprAllTargets crispr10K Cas9 target sites restricted to exons and 10 kb of flanking sequence
 
 hs1 refSeqComposite xenoRefGene RefSeq transcripts from other species, aligned to the human genome
 hs1 xenoRefGene refSeqComposite Human RefSeq transcripts, rather than transcripts from other species
 
 danRer11 refSeqComposite xenoRefGene RefSeq transcripts from other species, aligned to the human genome
 danRer11 xenoRefGene refSeqComposite Human RefSeq transcripts, rather than transcripts from other species
 
 # Map and assembly cross-links:
-hg38 ~t2tChain chainNetHs1 Another alignment of the T2T CHM13 assembly to GRCh38
 hg38 ~t2tChain chm13LiftOver Another alignment of the T2T CHM13 assembly to GRCh38
 hg38 problematic LCRs Low-complexity regions measured by longdust, another common source of alignment artifacts
 hg38 LCRs problematic Curated regions that often cause artifacts in sequencing and alignment
 hg38 hg38Patch11 patchesPsl Alignments of the patch and alt sequences to the primary assembly
 hg38 patchesPsl hg38Patch11 The patch and alternate sequences themselves, as placed on the assembly
 hg38 exomeProbesets genotypeArrays Microarray probesets and optical genome mapping sites
 hg38 genotypeArrays exomeProbesets Exome capture kit target regions and probe positions
-hg38 ~cloneEndSuper cloneEndUcsc Another mapping of the same clone library end sequences
 
 hg19 exomeProbesets genotypeArrays Microarray probesets and optical genome mapping sites
 hg19 genotypeArrays exomeProbesets Exome capture kit target regions and probe positions
 
 hs1 problematic LCRs Low-complexity regions measured by longdust, another common source of alignment artifacts
 hs1 LCRs problematic Curated regions that often cause artifacts in sequencing and alignment
 
 # Comparative genomics cross-links:
 hg38 unusualcons cons100way The vertebrate conservation scores these unusually conserved regions are called from
 hg38 cons100way unusualcons Ultraconserved elements, human accelerated regions and similar features
 hg38 gerp cons100way UCSC conservation scores from a 100-species vertebrate alignment
 hg38 cons100way gerp Conservation scores from Ensembl, computed on a 65-amniote alignment
 hg38 ~cons241way cons447way Another Zoonomia mammalian alignment, built on a different species set
 
 # Mouse gene and regulation cross-links:
 mm39 ~TOGAv2 HLTOGAannotvHg38v1 Another TOGA annotation projection, from a different release
 mm39 knownGene wgEncodeGencodeSuper All transcripts from each GENCODE release, including sets never used as the default gene track
 mm39 wgEncodeGencodeSuper knownGene The current default gene set
 mm39 ~liftOverMm10 grcIncidentDb Assembly changes between the mouse assemblies, and why they were made
 
 mm10 >knownGeneOld11 knownGene The newer version of this track
 mm10 ~TOGAv2 HLTOGAannotvHg38v1 Another TOGA annotation projection, from a different release
 mm10 epdNew fantom5 Transcription start sites and their usage, measured by CAGE
 mm10 fantom5 epdNew Experimentally supported promoters curated in EPDnew
 mm10 tabulaMuris tabulaMurisSenis The same single-cell atlas extended across the mouse lifespan
 mm10 tabulaMurisSenis tabulaMuris Single-cell expression across adult mouse organs, the basis of the Senis atlas
 
 # hs1 cross-links:
 hs1 varFreqs phasedVars Projects that provide haplotype-phased genotypes and variants
 hs1 phasedVars varFreqs Projects where variant frequencies, aka allele frequencies, are publicly available
 hs1 ~mappability problematic Regions that are hard to align to, and that often produce artifacts
 hs1 ~sedefSegDups censat Another class of highly repetitive sequence resolved by the T2T assembly
 hs1 ~simpleRepeat microsatellites Another annotation of short tandem repeats in the reference sequence
 
 # danRer11 cross-links:
 danRer11 >transMapV5 transMapV6 The current version of the TransMap alignments
 danRer11 ensGene refSeqComposite Gene models from NCBI RefSeq, curated independently of Ensembl
 danRer11 refSeqComposite ensGene Gene models from Ensembl, curated independently of RefSeq
 danRer11 ~simpleRepeat microsat Another annotation of short tandem repeats in the reference sequence
 
 # Repeat annotation cross-links:
 hg38 rmsk nestedRepeats Fragments of the same repeats joined by RepeatMasker ID, showing which pieces belong together
 hg38 nestedRepeats rmsk The individual repeat annotations these fragments were joined from
 hg38 rmsk joinedRmsk A detailed view of the same annotations, showing the alignment structure of each repeat
 hg38 joinedRmsk rmsk The standard view of these annotations, one item per repeat
 hg38 rmsk simpleRepeat Tandem repeats found by TRF, rather than the interspersed repeat families
 hg38 simpleRepeat rmsk Interspersed repeats and low-complexity DNA, annotated by family
 hg38 rmsk windowmaskerSdust An alternative masking of repetitive and low-complexity sequence, computed without a repeat library
 hg38 windowmaskerSdust rmsk Repeats annotated by family from a curated library, rather than found de novo
 
 hg19 rmsk nestedRepeats Fragments of the same repeats joined by RepeatMasker ID, showing which pieces belong together
 hg19 nestedRepeats rmsk The individual repeat annotations these fragments were joined from
 hg19 rmsk simpleRepeat Tandem repeats found by TRF, rather than the interspersed repeat families
 hg19 simpleRepeat rmsk Interspersed repeats and low-complexity DNA, annotated by family
 hg19 rmsk windowmaskerSdust An alternative masking of repetitive and low-complexity sequence, computed without a repeat library
 hg19 windowmaskerSdust rmsk Repeats annotated by family from a curated library, rather than found de novo
 
 mm39 rmsk nestedRepeats Fragments of the same repeats joined by RepeatMasker ID, showing which pieces belong together
 mm39 nestedRepeats rmsk The individual repeat annotations these fragments were joined from
 mm39 rmsk simpleRepeat Tandem repeats found by TRF, rather than the interspersed repeat families
 mm39 simpleRepeat rmsk Interspersed repeats and low-complexity DNA, annotated by family
 mm39 rmsk windowmaskerSdust An alternative masking of repetitive and low-complexity sequence, computed without a repeat library
 mm39 windowmaskerSdust rmsk Repeats annotated by family from a curated library, rather than found de novo
 
 mm10 rmsk nestedRepeats Fragments of the same repeats joined by RepeatMasker ID, showing which pieces belong together
 mm10 nestedRepeats rmsk The individual repeat annotations these fragments were joined from
 mm10 rmsk joinedRmsk A detailed view of the same annotations, showing the alignment structure of each repeat
 mm10 joinedRmsk rmsk The standard view of these annotations, one item per repeat
 mm10 rmsk simpleRepeat Tandem repeats found by TRF, rather than the interspersed repeat families
 mm10 simpleRepeat rmsk Interspersed repeats and low-complexity DNA, annotated by family
 mm10 rmsk windowmaskerSdust An alternative masking of repetitive and low-complexity sequence, computed without a repeat library
 mm10 windowmaskerSdust rmsk Repeats annotated by family from a curated library, rather than found de novo
 
 danRer11 rmsk nestedRepeats Fragments of the same repeats joined by RepeatMasker ID, showing which pieces belong together
 danRer11 nestedRepeats rmsk The individual repeat annotations these fragments were joined from
 danRer11 rmsk simpleRepeat Tandem repeats found by TRF, rather than the interspersed repeat families
 danRer11 simpleRepeat rmsk Interspersed repeats and low-complexity DNA, annotated by family
 danRer11 rmsk windowmaskerSdust An alternative masking of repetitive and low-complexity sequence, computed without a repeat library
 danRer11 windowmaskerSdust rmsk Repeats annotated by family from a curated library, rather than found de novo
 
 # Literature and association cross-links:
 hg38 gwasCatalog varsInPubs Individual variants mentioned in the literature, text-mined from full-text papers
 hg38 varsInPubs gwasCatalog Trait and disease associations from published genome-wide association studies
 hg38 gwasCatalog snpedia Wiki summaries of what has been published about individual SNPs
 hg38 snpedia gwasCatalog The underlying published associations, with effect sizes and p-values
 hg38 gwasCatalog gtexEqtlHighConf Variants that change gene expression, often used to find the gene behind an association signal
 hg38 gtexEqtlHighConf gwasCatalog Trait and disease association signals these expression effects are usually compared against
 hg38 snpedia varsInPubs Individual variants mentioned in the literature, text-mined from full-text papers
 hg38 varsInPubs snpedia Wiki summaries of what has been published about individual SNPs
 
 hg19 gwasCatalog varsInPubs Individual variants mentioned in the literature, text-mined from full-text papers
 hg19 varsInPubs gwasCatalog Trait and disease associations from published genome-wide association studies
 hg19 gwasCatalog snpedia Wiki summaries of what has been published about individual SNPs
 hg19 snpedia gwasCatalog The underlying published associations, with effect sizes and p-values
 hg19 snpedia varsInPubs Individual variants mentioned in the literature, text-mined from full-text papers
 hg19 varsInPubs snpedia Wiki summaries of what has been published about individual SNPs
 
 # Variant impact predictor cross-links:
 hg38 mutScore primateAi A pathogenicity predictor that also works from 3D protein structure
 hg38 primateAi mutScore Missense variant clustering within 3D protein structures
 hg38 mutScore revel An ensemble missense pathogenicity score built from multiple predictors
 hg38 revel mutScore Missense variant clustering within 3D protein structures
 hg38 mutScore alphaMissense A deep-learning missense pathogenicity predictor
 hg38 alphaMissense mutScore Missense variant clustering within 3D protein structures
 hg38 mutScore clinPred An ensemble missense pathogenicity predictor that incorporates gnomAD allele frequency
 hg38 clinPred mutScore Missense variant clustering within 3D protein structures
 hg38 >caddSuper1_7 revel An ensemble pathogenicity score for coding variants
 hg38 >caddSuper1_7 clinPred An ensemble missense pathogenicity predictor that incorporates gnomAD allele frequency
 hg38 >caddSuper1_7 alphaMissense A deep-learning missense pathogenicity predictor
 hg38 >caddSuper1_7 gnomadVariants Population allele frequencies, useful for judging whether a high-scoring variant is common
 
 hg19 >caddSuper1_7 gnomadSuper Population allele frequencies, useful for judging whether a high-scoring variant is common
 hg19 mutScore primateAi A pathogenicity predictor that also works from 3D protein structure
 hg19 primateAi mutScore Missense variant clustering within 3D protein structures
 hg19 mutScore revel An ensemble missense pathogenicity score built from multiple predictors
 hg19 revel mutScore Missense variant clustering within 3D protein structures
 hg19 mutScore alphaMissense A deep-learning missense pathogenicity predictor
 hg19 alphaMissense mutScore Missense variant clustering within 3D protein structures
 hg19 mutScore clinPred An ensemble missense pathogenicity predictor that incorporates gnomAD allele frequency
 hg19 clinPred mutScore Missense variant clustering within 3D protein structures
 hg19 >caddSuper1_7 revel An ensemble pathogenicity score for coding variants
 hg19 >caddSuper1_7 clinPred An ensemble missense pathogenicity predictor that incorporates gnomAD allele frequency
 hg19 >caddSuper1_7 alphaMissense A deep-learning missense pathogenicity predictor
 
 # Splicing impact cross-links:
 hg38 ~spliceAI abSplice Another deep-learning predictor of splice-altering variants
 hg38 spliceAI spliceVarDb Splicing variants with experimental validation, useful for checking these predictions
 hg38 spliceVarDb spliceAI Predicted splice-altering effects, scored genome-wide
 hg38 spliceAI spliceAIWt The same model run on the reference sequence, showing where splicing is expected without any variant
 hg38 spliceAIWt spliceAI The same model scored for variants, rather than for the reference sequence
 hg38 abSplice spliceVarDb Splicing variants with experimental validation, useful for checking these predictions
 hg38 spliceVarDb abSplice Predicted aberrant splicing, scored per variant and tissue
 hg38 spliceImpactSuper predictionScoresSuper Pathogenicity scores for coding and non-coding variants generally, not only splicing
 hg38 predictionScoresSuper spliceImpactSuper Prediction scores and databases for variants that disrupt splicing
 hg38 nmd spliceImpactSuper Predicted and validated splice-altering variants, a common source of premature termination codons
 hg38 spliceImpactSuper nmd Regions where premature termination codons are predicted to escape nonsense-mediated decay
 
 hg19 ~spliceAI abSplice Another deep-learning predictor of splice-altering variants
 hg19 spliceImpactSuper predictionScoresSuper Pathogenicity scores for coding and non-coding variants generally, not only splicing
 hg19 predictionScoresSuper spliceImpactSuper Prediction scores and databases for variants that disrupt splicing
 
 # Constraint score cross-links:
 hg38 constraintSuper predictionScoresSuper Per-variant deleteriousness and pathogenicity scores, rather than regional constraint
 hg38 predictionScoresSuper constraintSuper Regional and gene-level constraint measured from population variation
 hg38 ~jarvis ukbDepletion Another score for how depleted of variation a non-coding region is
 hg38 ~hmc gnomadPLI Another constraint metric derived from the absence of variation in population data
 hg38 hmc ucscGenePfam The Pfam domains that homologous missense constraint is calculated over
 hg38 ucscGenePfam hmc Missense constraint measured across homologous positions within these domains
 hg38 promoterAi jarvis A score prioritizing non-coding regions more broadly, not only promoters
 hg38 jarvis promoterAi A deep-learning predictor for variants in promoter regions specifically
 
 hg19 constraintSuper predictionScoresSuper Per-variant deleteriousness and pathogenicity scores, rather than regional constraint
 hg19 predictionScoresSuper constraintSuper Regional and gene-level constraint measured from population variation
 hg19 ~jarvis ukbDepletion Another score for how depleted of variation a non-coding region is
 hg19 ~hmc gnomadPLI Another constraint metric derived from the absence of variation in population data
 hg19 hmc ucscGenePfam The Pfam domains that homologous missense constraint is calculated over
 hg19 ucscGenePfam hmc Missense constraint measured across homologous positions within these domains