7f892f8fa5f41b18d489cfdbb0255c05b1b3e3f3
jnavarr5
  Mon Oct 7 10:55:15 2019 -0700
Updating http to https for hg19, uiLinks cronjob.

diff --git src/hg/makeDb/trackDb/human/hiSeqDepth.html src/hg/makeDb/trackDb/human/hiSeqDepth.html
index 68ff08f..c9f1f2b 100644
--- src/hg/makeDb/trackDb/human/hiSeqDepth.html
+++ src/hg/makeDb/trackDb/human/hiSeqDepth.html
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 <H1>Description</H1>
 <P>
 This track displays regions of the reference genome that have exceptionally high
 sequence depth, inferred from alignments of short-read sequences from the
-<A HREF="http://www.internationalgenome.org/" TARGET="_blank">1000 Genomes Project</A>.
+<A HREF="https://www.internationalgenome.org/" TARGET="_blank">1000 Genomes Project</A>.
 These regions may be caused by collapsed repetitive sequences
 in the reference genome assembly; they also have high read depth in assays such as
 ChIP-seq, and may trigger false positive calls from peak-calling algorithms.
 Excluding these regions from analysis of short-read alignments should reduce
 such false positive calls.
 </P>
 
 <H1>Methods</H1>
 <P>
 Pickrell <em>et al.</em> downloaded sequencing reads for 57 Yoruba individuals
 from the 1000 Genomes Project's low-coverage pilot data, mapped them to the
 Mar. 2006 human genome assembly (NCBI36/hg18), computed the read depth for
 every base in the genome, and compiled a distribution of read depths.
 They then identified contiguous regions where read depth exceeded thresholds
 corresponding to the top 0.001, 0.005, 0.01, 0.05 and 0.1 of the per-base