5cfc2f6577687733dcfc56c3f745e7799d200998
ccpowell
  Tue Jun 4 15:59:41 2019 -0700
Editing hg38 link on the encRegTfbsClustered.html page, refs #21139

diff --git src/hg/makeDb/trackDb/human/encRegTfbsClustered.html src/hg/makeDb/trackDb/human/encRegTfbsClustered.html
index 9de3cf4..6767c1a 100644
--- src/hg/makeDb/trackDb/human/encRegTfbsClustered.html
+++ src/hg/makeDb/trackDb/human/encRegTfbsClustered.html
@@ -10,31 +10,31 @@
 regulate gene expression.  Some TFs contain a DNA binding domain and can bind directly to 
 specific short DNA sequences ('motifs');
 others bind to DNA indirectly through interactions with TFs containing a DNA binding domain.
 High-throughput antibody capture and sequencing methods (e.g. chromatin immunoprecipitation
 followed by sequencing, or 'ChIP-seq') can be used to identify regions of
 TF binding genome-wide.  These regions are commonly called ChIP-seq peaks.</p>
 <p>
 ENCODE TF ChIP-seq data were processed using the 
 <a target="_blank" href="https://www.encodeproject.org/chip-seq/transcription_factor/">ENCODE Transcription Factor ChIP-seq Processing Pipeline</a> to generate peaks of TF binding.
 Peaks from 1264 experiments (1256 in hg38) representing 338 transcription factors 
 (340 in hg38) in 130 cell types (129 in hg38) are combined here into clusters to produce a 
 summary display showing occupancy regions for each factor.
 The underlying ChIP-seq peak data are available from the
 <i>ENCODE 3 TF ChIP Peaks</i> tracks (
 <a target="_blank" href="../cgi-bin/hgTrackUi?db=hg19&g=encTfChipPk">hg19</a>,
-<a target="_blank" href="../cgi-bin/hgTrackUi?db=hg19&g=encTfChipPk">hg38</a>)</p>
+<a target="_blank" href="../cgi-bin/hgTrackUi?db=hg38&g=encTfChipPk">hg38</a>)</p>
 
 <h2>Display Conventions</h2>
 <p>
 A gray box encloses each peak cluster of transcription factor occupancy, with the
 darkness of the box being proportional to the maximum signal strength observed in any cell type
 contributing to the cluster. The HGNC gene name for the transcription factor is shown 
 to the left of each cluster.<p>
 <p>
 To the right of the cluster a configurable label can optionally display information about the
 cell types contributing to the cluster and how many cell types were assayed for the factor
 (count where detected / count where assayed).
 For brevity in the display, each cell type is abbreviated to a single letter.
 The darkness of the letter is proportional to the signal strength observed in the cell line. 
 Abbreviations starting with capital letters designate
 <a href="https://www.encodeproject.org/search/?type=Biosample&organism.scientific_name=Homo+sapiens"