198c9b8daecc44fbda6a6494c566c723920f030a
lrnassar
  Wed Mar 11 18:25:21 2026 -0700
Fixing a few hundred clear typos with the help of Claude. Some are less important in code comments, but majority of them are in user-facing places. I manually approved 60%+ of the changes and didn't see any that were an incorrect suggestion, at worst it was potentially uncessesary, like a code comment having cant instead of can't. No RM.

diff --git src/hg/makeDb/trackDb/human/hg19/gnomad.html src/hg/makeDb/trackDb/human/hg19/gnomad.html
index ed4016e50bd..d6914d7ac79 100644
--- src/hg/makeDb/trackDb/human/hg19/gnomad.html
+++ src/hg/makeDb/trackDb/human/hg19/gnomad.html
@@ -38,31 +38,31 @@
 on 10,847 unrelated genomes.</li>
 <li><a href="/cgi-bin/hgTrackUi?db=hg19&g=gnomadPLI"><strong>Predicted Constraint 
 Metrics (gnomAD Constraint Metrics)</strong></a> - Contains metrics of 
 pathogenicity per-gene as predicted for gnomAD v2.1.1.</li>
 <li><a href="/cgi-bin/hgTrackUi?db=hg19&g=gnomadMpc">
 <strong>Missense Deleteriousness Prediction by Constraint (MPC)</strong></a> - Regions of
 transcripts (not entire transcripts) that show enrichment of missense mutations.</li></ul>
 </p>
 
 <h2>Display Conventions</h2>
 <p>
 These tracks are multi-view composite tracks that contain multiple data types (views). Each view
 within a track has separate display controls, as described <a target="_blank"
 href="https://genome.ucsc.edu/goldenPath/help/multiView.html">here</a>. Most gnomAD tracks contain
 multiple subtracks, corresponding to subsets of data. If a track contains many subtracks, only some
-subracks will be displayed by default. The user can select which subtracks are displayed via the
+subtracks will be displayed by default. The user can select which subtracks are displayed via the
 display controls on the track details page.
 </p> 
 
 <h2>Data Access</h2>
 <p>
 The raw data can be explored interactively with the <a target="_blank" href="../cgi-bin/hgTables">
 Table Browser</a>, or the <a target="_blank" href="../cgi-bin/hgIntegrator">Data Integrator</a>. For
 automated analysis, the data may be queried from our <a target="_blank" 
 href="/goldenPath/help/api.html">REST API</a>, and the genome annotations are stored in files that 
 can be downloaded from our <a
 href="http://hgdownload.soe.ucsc.edu/gbdb/$db/gnomAD/" target="_blank">download server</a>, subject
 to the conditions set forth by the gnomAD consortium (see below). Coverage values
 for the genome are in <a target="_blank" href="../goldenPath/help/bigWig.html">bigWig</a> files in
 the coverage/ subdirectory. Variant VCFs can be found in the vcf/ subdirectory.</p>
 <p>