10be0991b45bc01981e68f72a660adbbcc999f77
jnavarr5
  Fri Sep 25 15:53:33 2026 -0700
Updating the filter paragraph on the track description page. Updating the defaultLabels since searching for a CpG ID would result in not showing that ID, refs #38112

diff --git src/hg/makeDb/trackDb/human/hg38/episignatures.ra src/hg/makeDb/trackDb/human/hg38/episignatures.ra
index d31cd18ba31..6b774bafbc8 100644
--- src/hg/makeDb/trackDb/human/hg38/episignatures.ra
+++ src/hg/makeDb/trackDb/human/hg38/episignatures.ra
@@ -46,31 +46,31 @@
     filterLabel.direction Direction and strength
 
     track epigenCentral
     parent episignatures
     shortLabel EpigenCentral
     longLabel EpigenCentral: CpG probes of curated DNA methylation episignatures
     type bigBed 9 +
     bigDataUrl /gbdb/hg38/episignatures/epigenCentral.bb
     visibility pack
     itemRgb on
     noScoreFilter on
     tableBrowser off
     maxWindowCoverage 10000000
     searchIndex name
     labelFields name,displaySignature
-    defaultLabelFields displaySignature
+    defaultLabelFields name,displaySignature
     skipFields signatureList
     detailsDynamicTable comparisonTable|Episignatures at this CpG site
     urls displayOmim="https://omim.org/entry/$$"
     mouseOver <b>Probe:</b> ${name}<br><b>Episignatures at this probe:</b> ${sigCount}<br><b>Strongest episignature:</b> ${displaySignature}<br><b>Disorder:</b> ${displayDisorder}<br><b>OMIM:</b> ${displayOmim}<br><b>Direction:</b> ${direction}<br><b>Absolute delta-beta:</b> ${maxAbsDelta}
     filterByRange.sigCount on
     filter.sigCount 1:6
     filterLimits.sigCount 1:6
     filterLabel.sigCount Number of episignatures at this probe
     filterValues.direction Gain,Loss
     filterType.direction multipleListOr
     filterLabel.direction Direction of methylation change
     filterValues.signatureList 16pDel|Autism spectrum (16pDel),ANKRD11|KBG syndrome (ANKRD11),ARID1B|Coffin-Siris syndrome 1 (ARID1B),ASXL1|Bohring-Opitz syndrome (ASXL1),CHD7|CHARGE syndrome (CHD7),CHD8|Intellectual developmental disorder with autism and macrocephaly (CHD8),Dup7|Chromosome 7q11.23 duplication syndrome (Dup7),DYRK1A|Intellectual developmental disorder; autosomal dominant 7 (DYRK1A),EHMT1|Kleefstra syndrome 1 (EHMT1),EZH2|Weaver syndrome (EZH2),FHS|Floating-Harbor syndrome (FHS),HNRNPK|Au-Kline syndrome (HNRNPK),KANSL1|Koolen-De Vries syndrome (KANSL1),KMT2A|Wiedemann-Steiner syndrome (KMT2A),KMT2B|Dystonia 28; childhood-onset (KMT2B),KMT2C|Kleefstra syndrome 2 (KMT2C),KMT2D_2017|Kabuki syndrome 1 (KMT2D_2017),KMT2D_2026|Kabuki syndrome 1 (KMT2D_2026),MN1|CEBALID syndrome (MN1),NSD1|Sotos syndrome (NSD1),SMARCA2|Nicolaides-Baraitser syndrome (SMARCA2),SRCAP|Developmental delay; hypotonia; musculoskeletal defects; and behavioral abnormalities (SRCAP),T21|Down syndrome (T21),Williams|Williams-Beuren syndrome (Williams)
     filterType.signatureList multipleListAnd
     filterLabel.signatureList Episignature