279143838dbbba19a628e2f0658bc856deba6c95
lrnassar
  Mon Oct 9 14:51:40 2023 -0700
Removing tracks from the covid bluebar group to make room for HPRC, refs #32213

diff --git src/hg/makeDb/trackDb/human/trackDb.ra src/hg/makeDb/trackDb/human/trackDb.ra
index bc5ae65..5510715 100644
--- src/hg/makeDb/trackDb/human/trackDb.ra
+++ src/hg/makeDb/trackDb/human/trackDb.ra
@@ -5591,31 +5591,32 @@
 semiShortCircuit 1
 termRegex nssv[0-9]+
 searchType bed
 searchPriority 50
 
 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: $inhMode
 labelFields gene, name
 defaultLabelFields gene, name
 noScoreFilter on
-group covid 
+priority 2.2
+group varRep
 color 179,0,0
 visibility hide
 bigDataUrl /gbdb/$D/covidMuts/covidMuts.bb
 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=$$" hgnc="https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/HGNC:$$"