28283c6fd389638ee667a24fb7e938c2222a4535
hiram
  Wed May 4 18:13:51 2022 -0700
correctly use $D in bigDataUrl path names so the track only shows up on the correct browser no redmine

diff --git src/hg/makeDb/trackDb/human/trackDb.ra src/hg/makeDb/trackDb/human/trackDb.ra
index cc6710b..97d3b6a 100644
--- src/hg/makeDb/trackDb/human/trackDb.ra
+++ src/hg/makeDb/trackDb/human/trackDb.ra
@@ -4769,42 +4769,42 @@
     view dose
     shortLabel ClinGen sensitivity
     longLabel ClinGen sensitivity composite track
     group phenDis
     visibility hide
     type bigBed 9 +
     itemRgb on
 
         track clinGenHaploInsufficiency
         parent doseSensitivity
         shortLabel Haplo Insufficiency
         longLabel ClinGen Haplo Insufficiency
         visibility dense
         priority 1
         type bigBed 9 +
-        bigDataUrl /gbdb/hg19/doseSensitivity/clinGenHaploInsufficiency.bb
+        bigDataUrl /gbdb/$D/doseSensitivity/clinGenHaploInsufficiency.bb
         mouseOverField mouseOver
         subGroups view=dose class=path level=cur
 
         track clinGenTriploSensitivity
         parent doseSensitivity
         shortLabel Triplo Sensitivity
         longLabel ClinGen Triplo Sensitivity
         visibility dense
         priority 2
         type bigBed 9 +
-        bigDataUrl /gbdb/hg19/doseSensitivity/clinGenTriploSensitivity.bb
+        bigDataUrl /gbdb/$D/doseSensitivity/clinGenTriploSensitivity.bb
         mouseOverField mouseOver
         subGroups view=dose class=path level=cur
 
 include phastBias.ra
 
 searchName decipherId
 searchTable decipher
 termRegex [0-9]+
 searchType bed
 searchPriority 50
 release public
 
 searchName decipherSnvsId
 searchTable decipherSnvs
 termRegex [0-9]+
@@ -5426,31 +5426,31 @@
 
 include covidHgiGwas.ra
 
 track covidMuts
 type bigBed 12 + 
 shortLabel Rare Harmful Vars
 longLabel Rare variants underlying COVID-19 severity and susceptibility from the COVID Human Genetics Effort
 mouseOver $gene $name $rsId Genotype: $genotype; Zygosity: $zygo ; Inheritance: $inhMode
 labelFields gene, name
 defaultLabelFields gene, name
 noScoreFilter on
 group covid 
 color 179,0,0
 visibility hide
 bigDataUrl /gbdb/$D/covidMuts/covidMuts.bb
-multiRegionsBedUrl /gbdb/hg19/covidMuts/covidMuts.regions.bed
+multiRegionsBedUrl /gbdb/$D/covidMuts/covidMuts.regions.bed
  
 track orphadata
 bigDataUrl /gbdb/$D/bbi/orphanet/orphadata.bb
 shortLabel Orphanet
 longLabel Orphadata: Aggregated Data From Orphanet
 group phenDis
 type bigBed 9 +
 bedNameLabel OrphaCode
 url http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=$$
 urlLabel OrphaNet Phenotype Link:
 urls ensemblID="https://grch37.ensembl.org/Homo_sapiens/Gene/Summary?db=core;g=$$" pmid="https://pubmed.ncbi.nlm.nih.gov/$$" orphaCode="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=$$" omim="https://www.omim.org/entry/$$?search=$$&highlight=$$" hgnc="https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/HGNC:$$"
 skipEmptyFields on
 skipFields name,score,itemRgb
 mouseOver Gene: $geneSymbol, Disorder: $disorder, Inheritance(s): $inheritance, Onset: $onsetList
 filterValues.assnType Biomarker tested in,Candidate gene tested in,Disease-causing germline mutation(s) (gain of function) in,Disease-causing germline mutation(s) (loss of function) in,Disease-causing germline mutation(s) in,Disease-causing somatic mutation(s) in,Major susceptibility factor in,Modifying germline mutation in,Part of a fusion gene in,Role in the phenotype of