2b5f10644f8fc336b6f73c10967edee119f8e8f3
gperez2
  Mon Apr 1 17:42:56 2024 -0700
Code review edits, refs #33313

diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html
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--- src/hg/htdocs/goldenPath/newsarch.html
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@@ -62,35 +62,33 @@
 
 <!-- ============= 2024 archived news ============= -->
 <a name="2024"></a>
 
 <a name="032624"></a>
 <h2>Mar. 26, 2024 &nbsp;&nbsp; New gnomAD v4 Constraint Metrics (hg38) and gnomAD Non-cancer filter (hg19/hg38)</h2>
 <p>
 We are pleased to announce the release of the
 <a href="/cgi-bin/hgTrackUi?&db=hg38&g=gnomadPLI">gnomAD v4 constraint metrics</a> for human
 assembly hg38/GRCh38 and the addition of a non-cancer filter for the
 <a href="/cgi-bin/hgTrackUi?db=hg19&g=gnomadExomes">GRCh37/hg19 Exome Variants v2.1.1</a> and the
 <a href="/cgi-bin/hgTrackUi?db=hg38&g=gnomadGenomesVariantsV3_1_1">
 hg38/GRCh38 Genome Variants v3.1.1</a> tracks.</p>
 <p>
 The gnomAD v4 constraint metrics tracks contain metrics of pathogenicity per-gene as predicted for
-gnomAD v4.0 and identifies genes subject to strong selection against various classes of mutation.
-These tracks contain metrics of pathogenicity per-gene as predicted for gnomAD v4.0 and
-identifies genes subject to strong selection against various classes of mutation. The release of
-the gnomAD v4 constraint metrics consists of two new subtracks in the gnomAD Constraint Metrics
-composite track:</p>
+gnomAD v4.0 and identify genes subject to strong selection against various classes of mutation.
+The release of the gnomAD v4 constraint metrics consists of two new subtracks in the gnomAD
+Constraint Metrics composite track:</p>
 <ol>
   <li><b>Transcript LoF Constraint track</b>: Predicted constraint metrics at the whole transcript
     level for three different types of variation: missense, synonymous, and predicted loss of
     function.</li>
   <li><b>Transcript Missense Constraint track</b>: The missense constraint tracks are built
     similarly to the LoF constraint tracks, however the items displayed are based on missense Z
     scores. All items are colored black, and individual Z scores can be seen on mouseover.
 </ol>
 <p>
 The GRCh37/hg19 Exome Variants v2.1.1 and the hg38/GRCh38 Genome Variants v3.1.1 tracks now have a
 non-cancer filter that allows the option to exclude/include variants from samples of individuals
 who were not ascertained for having cancer in a cancer study. These non-cancer subsets follow the
 new guidelines for clinical variant testing of BRCA1 and BRCA2 genes and are used for the
 assessment of breast cancer patients.</p>
 <p>