10f0f6d5160a96867ecf534e1b9d138df7d9b796
lrnassar
  Mon Sep 28 16:17:46 2026 -0700
Fiber-seq: hide the container by default, and split the five GM lines out
into a Rare disease sample class.  Max asked for superTrack on rather than
on show, since the track covers much the same ground as ENCODE DNase and
does not earn a slot in everyone's default hg38 view.  The five
lymphoblastoid lines GM25455, GM25456, GM27730, GM28570 and GM28572 had
been filed as Common Cell Line; Andrew Stergachis says they are rare
disease cases consented to broad genomic data sharing and the first of a
batch the lab intends to keep adding, so SAMPLE_CLASS_COLORS gains a third
entry and the facet now reads 20 HPRC, 16 Common Cell Line, 5 Rare disease
sample.  refs #36210

diff --git src/hg/makeDb/trackDb/human/hg38/fiberSeq.ra src/hg/makeDb/trackDb/human/hg38/fiberSeq.ra
index 9c4d21cf0ce..c4a2cfc3e4c 100644
--- src/hg/makeDb/trackDb/human/hg38/fiberSeq.ra
+++ src/hg/makeDb/trackDb/human/hg38/fiberSeq.ra
@@ -1,22 +1,22 @@
 # Fiber-seq: chromatin accessibility, FIRE regulatory elements and CpG
 # methylation from PacBio HiFi Fiber-seq, Stergachis and Vollger labs.
 # Generated by hg/makeDb/scripts/fiberSeq/fiberSeqTrackDb.py.
 # Do not edit by hand, edit the script and regenerate.
 
 track fiberSeq
-superTrack on show
+superTrack on
 shortLabel Fiber-seq
 longLabel Fiber-seq chromatin accessibility, regulatory elements and CpG methylation
 group regulation
 priority 2.5
 
     track fiberSeqAcc
     parent fiberSeq
     container multiWig
     aggregate transparentOverlay
     showSubtrackColorOnUi on
     type bigWig 0 100
     viewLimits 0:100
     autoScale off
     alwaysZero on
     graphTypeDefault bar