ca100016955e808effb386de2e8905b9473790f3
jnavarr5
  Wed Mar 18 15:04:03 2026 -0700
Editing the relatedTracks text shown for each STR track for hg38, refs #36652 #35420

diff --git src/hg/makeDb/trackDb/relatedTracks.ra src/hg/makeDb/trackDb/relatedTracks.ra
index 11190ea044b..973c22d1151 100644
--- src/hg/makeDb/trackDb/relatedTracks.ra
+++ src/hg/makeDb/trackDb/relatedTracks.ra
@@ -2,32 +2,32 @@
 # ucscDb track trackLinkingTo reason
 
 # 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 gnomad View associated variants
 hg38 gnomad 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 gnomadStr strVar gnomAD STR genotypes at disease-associated loci; STR Variation supertrack has population-level STR data
-hg38 strVar gnomadStr Population-level STR variation; gnomAD STR track has disease-associated locus genotypes
+hg38 gnomadStr strVar A collection of population-level STR variation tracks across the genome
+hg38 strVar gnomadStr Population-level STR variation across disease-associated loci from gnomAD v3.1.3
 
 hg38 revel liftHg38 Revel is based on hg19 and lifted to hg38. liftOver "chain" alignment from hg19 to hg38
 hg38 liftHg38 revel Revel scores were lifted using UCSC liftOver chains from hg38
 
 hg38 revel caddSuper CADD, a similar deleteriousness score, and not used as an input by REVEL
 hg38 caddSuper revel REVEL, a similar deleteriousness score
 
 hg38 liftHg19 grcIncidentDb GRC Incident database, to explore reasons why the assembly was changed
 hg38 grcIncidentDb liftHg19 LiftOver for hg38, explores how incident regions aligned between 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 ReMap, even though it has the same name, is a database of transcription factor binding sites, unrelated to NCBI ReMap
 
 hg38 ReMap jaspar JASPAR is a database of predicted TF binding sites, based on short DNA matches. Unlike ReMap, the data is purely computational.