29c3c9a501f6cdefcc8e155f075523eb73e15ec9
lrnassar
  Thu Jul 16 18:25:15 2026 -0700
Uncommenting the staged ENCODE4 announcement now that long-read SVs is released, refs #37845

diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html
index 39e6430dd7a..708f5509089 100644
--- src/hg/htdocs/goldenPath/newsarch.html
+++ src/hg/htdocs/goldenPath/newsarch.html
@@ -52,32 +52,30 @@
 <p>You can sign-up to get these announcements via our 
 <a target=_blank href="https://groups.google.com/a/soe.ucsc.edu/g/genome-announce?hl=en">Genome-announce</a>
 email list. We send around one short announcement email every two weeks.</p>
 
 <p>Smaller software changes are not announced here.  A summary of the three-weekly release changes can be 
 found <a target=_blank href="https://genecats.gi.ucsc.edu/builds/versions.html">here</a>. 
 For the full list of our daily code changes head to our <a
 href="https://github.com/ucscGenomeBrowser/kent/commits/master"
 target=_blank>GitHub page</a>. Lastly, see our <a href="credits.html" target="_blank">
 credits page</a> for acknowledgments of the data we host.</p>
 
 <!-- ============= 2026 archived news ============= -->
 
 <a name="2026"></a>
 
-
-<!-- Hidden until ready to announce, refs #37845
 <a name="072226"></a>
 <h2>Jul. 22, 2026 &nbsp;&nbsp; ENCODE4 cCREs and ENCODE4 Regulation tracks released for human (hg38) and mouse (mm10)</h2>
 <p>
 We are excited to announce our major release of the ENCODE4 data collection on the
 UCSC Genome Browser for both the human (hg38/GRCh38) and mouse (mm10/GRCm38)
 assemblies. This release consists of two major components: the
 <a href="/cgi-bin/hgTrackUi?db=hg38&c=chr7&g=cCREs&position=default" target="_blank">
 <b>ENCODE Registry of cCREs</b></a> (candidate Cis-Regulatory Elements) container,
 and the new
 <a href="/cgi-bin/hgTrackUi?db=hg38&c=chr7&g=wgEncodeReg4&position=default" target="_blank">
 <b>ENCODE4 Regulation</b></a> container, both described in
 <a href="https://www.nature.com/articles/s41586-025-09909-9" target="_blank">
 Moore <em>et al</em>., <em>Nature</em> 2026</a>.
 </p>
 
@@ -273,31 +271,30 @@
 Transcriptional Regulation</a>. <em>Nature</em>. 2026 January 7.
 PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/39763870" target="_blank">39763870</a>;
 PMC: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11703161/" target="_blank">PMC11703161</a>.
 </p>
 
 <p>
 This dataset was produced by the ENCODE Data Analysis Center
 (<a href="https://www.umassmed.edu/zlab/" target="_blank">Weng lab</a> at
 UMass Chan Medical School). Major kudos to Mingshi Gao, Jill Moore, and Zhiping Weng for creating and
 improving the expansive track hubs for ENCODE4 and for iterating with us to
 bring them to the browser as native tracks. We also thank the ENCODE Consortium, the ENCODE production
 laboratories, and the ENCODE Data Coordination Center for generating and
 processing the underlying experiments, and Gerardo Perez, Brian Raney, Max
 Haeussler, and Lou Nassar for building and reviewing these tracks.
 </p>
--->
 
 <a name="071626"></a>
 <h2>Jul. 16, 2026 &nbsp;&nbsp; Long-read Structural Variants tracks for human (hg38 and hs1)</h2>
 <p>
 We are excited to announce a new
 <a href="/cgi-bin/hgTrackUi?db=hg38&g=longReadVariants&position=default" target="_blank"><b>Long-read
 Structural Variants</b></a> container track on the human assemblies
 <a href="/cgi-bin/hgTrackUi?db=hg38&g=longReadVariants&position=default" target="_blank">GRCh38/hg38</a> and
 <a href="/cgi-bin/hgTracks?db=hs1&position=default" target="_blank">T2T-CHM13/hs1</a>.
 The container track brings together structural variant (SV) callsets from 14 long-read
 sequencing studies worldwide into a single place where you can compare large genomic
 rearrangements (deletions, insertions, duplications, inversions, and complex events)
 across populations, cohorts, and calling strategies. Long-read technologies span
 repetitive regions and resolve complex loci that are difficult to detect with short
 reads, giving more precise breakpoints and better sensitivity for large variants.