1bad8b54aabb3a9e40df9eb92fdda92d1a6af379
braney
  Wed Nov 27 10:24:53 2019 -0800
add showCfg trackDb variable to automatically open hgTrackUi view
configurations

diff --git src/hg/makeDb/trackDb/human/trackDb.ra src/hg/makeDb/trackDb/human/trackDb.ra
index 98ea355..2d2e999 100644
--- src/hg/makeDb/trackDb/human/trackDb.ra
+++ src/hg/makeDb/trackDb/human/trackDb.ra
@@ -1627,30 +1627,31 @@
 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 pack
     type bigDbSnp
     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,\
         freqIncomplete|Frequency reported with incomplete allele data,\
         freqIsAmbiguous|Frequency reported for allele with IUPAC ambiguous base(s),\
         freqNotMapped|Frequency reported on different assembly but not mapped by dbSNP,\
         freqNotRefAlt|Reference genome allele is not major allele in at least one project,\