de2cb47114dbcf3ae57ac372bb2cab0263a3e9c5
chmalee
  Thu Oct 14 15:46:17 2021 -0700
Restoring pre-emptive removal of detailsTabUrls setting, which fixes crispr, snp153 and gnomad tracks, refs #28335

diff --git src/hg/makeDb/trackDb/human/trackDb.ra src/hg/makeDb/trackDb/human/trackDb.ra
index e7b8f3c..2a3a571 100644
--- src/hg/makeDb/trackDb/human/trackDb.ra
+++ src/hg/makeDb/trackDb/human/trackDb.ra
@@ -1594,31 +1594,31 @@
 defaultGeneTracks knownGene
 maxWindowToDraw 10000000
 type bed 6 +
 trackHandler snp125
 chimpOrangMacOrthoTable snp151OrthoPt5Pa2Rm8
 chimpDb panTro5
 orangDb ponAbe2
 macaqueDb rheMac8
 hapmapPhase III
 codingAnnotations snp151CodingDbSnp,
 
 #track dbSnp152
 #shortLabel All dbSNP (152)
 #longLabel Short Genetic Variants from dbSNP release 152
 #bigDataUrl /gbdb/$D/snp/dbSnp152.bb
-#detailsUrls _dataOffset=/gbdb/hgFixed/dbSnp/dbSnp152Details.tab.gz
+#detailsTabUrls _dataOffset=/gbdb/hgFixed/dbSnp/dbSnp152Details.tab.gz
 #group varRep
 #visibility hide
 #url https://www.ncbi.nlm.nih.gov/snp/$$
 #urlLabel dbSNP: 
 #type bigDbSnp
 #freqSourceOrder 1000Genomes,GnomAD_exomes,TOPMED,GnomAD,ExAC,GoESP,ALSPAC,TWINSUK,Estonian
 #maxWindowToDraw 1000000
 #classFilterValues snv,mnv,ins,del,delins,identity
 #classFilterType multipleListOr
 #ucscNotesFilterValues |(nothing noted),classMismatch|Variant class/type is inconsistent with allele sizes,clinvar|Present in ClinVar,clusterError|Overlaps a variant with the same type/class and position,commonAll|MAF >= 1% in all projects that report frequencies,commonSome|MAF >= 1% in at least one project that reports frequencies,delMismatch|Deleted sequence mismatches genomic reference sequence,diffMajor|Different projects report different major alleles,multiMap|Variant is placed in more than one genomic position,overlapDiffClass|Variant overlaps other variant(s) of different type/class,overlapSameClass|Variant overlaps other variant(s) of same type/class but different position,refIsMinor|Genomic reference allele is minor allele in at least one project that reports frequencies,refIsRare|Genomic reference allele frequency is <1% in at least one project,refIsSingleton|Genomic reference frequency is 0 in all projects reporting frequencies,revStrand|Variant maps to opposite strand relative to dbSNP's preferred top-level placement
 #ucscNotesFilterType multipleListOr
 #maxFuncImpactFilterValues 0|(not annotated),0865|frameshift,1587|stop_gained,1574|splice_acceptor_variant,1575|splice_donor_variant,1821|inframe_insertion,1583|missense_variant,1590|terminator_codon_variant,1819|synonymous_variant,1580|coding_sequence_variant,1623|5_prime_UTR_variant,1624|3_prime_UTR_variant,1619|nc_transcript_variant,2153|genic_upstream_transcript_variant,1986|upstream_transcript_variant,2152|genic_downstream_transcript_variant,1987|downstream_transcript_variant,1627|intron_variant
 #maxFuncImpactFilterType multipleListOr
 #priority 6.8
 #release alpha
@@ -1629,31 +1629,31 @@
 longLabel Short Genetic Variants from dbSNP release 153
 type bed 3
 group varRep
 visibility pack
 url https://www.ncbi.nlm.nih.gov/snp/$$
 urlLabel dbSNP: 
 subGroup1 view Views variants=Variants errs=Mapping_Errors
 priority 0.8
 
     track dbSnp153ViewVariants
     view variants
     parent dbSnp153Composite
     shortLabel Variants
     visibility dense
     type bigDbSnp
-    detailsUrls _dataOffset=/gbdb/hgFixed/dbSnp/dbSnp153Details.tab.gz
+    detailsTabUrls _dataOffset=/gbdb/hgFixed/dbSnp/dbSnp153Details.tab.gz
     freqSourceOrder 1000Genomes,GnomAD_exomes,TOPMED,ExAC,PAGE_STUDY,GnomAD,GoESP,Estonian,ALSPAC,TWINSUK,NorthernSweden,Vietnamese
     classFilterValues snv,mnv,ins,del,delins,identity
     classFilterType multipleListOr
     showCfg on
     ucscNotesFilterValues \
         altIsAmbiguous|Alternate allele contains IUPAC ambiguous base(s),\
         classMismatch|Variant class/type is inconsistent with allele sizes,\
         clinvar|Present in ClinVar,\
         clinvarBenign|ClinVar significance of benign and/or likely benign,\
         clinvarConflicting|ClinVar includes both benign and pathogenic reports,\
         clinvarPathogenic|ClinVar significance of pathogenic and/or likely pathogenic,\
         clusterError|Overlaps a variant with the same type/class and position,\
         commonAll|MAF >= 1% in all projects that report frequencies,\
         commonSome|MAF >= 1% in at least one project that reports frequencies,\
         diffMajor|Different projects report different major alleles,\