8e22e6e2afe9bb9df058ba48430a679702e79391
dschmelt
  Fri Jul 31 15:22:29 2020 -0700
Minor type fix #18419

diff --git src/hg/makeDb/trackDb/human/omimGene2.html src/hg/makeDb/trackDb/human/omimGene2.html
index 9078352..e9bb83e 100644
--- src/hg/makeDb/trackDb/human/omimGene2.html
+++ src/hg/makeDb/trackDb/human/omimGene2.html
@@ -152,31 +152,31 @@
 that can be used to retrieve data in JSON format from a particular chromosome range.</p>
 
 <p>
 Please refer to our searchable
 <A HREF="https://groups.google.com/a/soe.ucsc.edu/forum/?hl=en&fromgroups#!search/download+snps"
 target=_blank>mailing list archives</a>
 for more questions and example queries, or our
 <a HREF="../FAQ/FAQdownloads.html#download36" target=_blank>Data Access FAQ</a>
 for more information.</p>
 
 <h4>Example: Retrieve phenotype, Mode of Inheritance, and other OMIM data within a range</h4>
 <ol>
 <li>Go to <a href="hgTables">Table Browser</a>, make sure the following options are selected:
 group: Phenotype and Literature, track: OMIM Genes, table: <tt>omimGene2</tt>.</li>
 <li>Enter coordinates or a gene symbol into the &quot;Position&quot; textbox, such as
-chr1:11,106,535-11,262,551 or MTOR.</li>
+chr1:11,166,591-11,322,608 or MTOR.</li>
 <li>Change the &quot;Output format&quot; dropdown to &quot;selected fields from primary 
 and related Tables&quot; and click <button>get output</button>. Instead of returning 
 the standard formatted dataset from the <tt>omimGene2</tt> table, this 
 bring up the data field and linked table selection page.</li>
 <li>Select chrom, chromStart, chromEnd,and name from omimGene2 table. Then select the related tables <tt>omim2gene</tt> 
 and <tt>omimPhenotype</tt> and click <button>allow selection from check tables</button>.
 This brings up the fields of the linked tables, where you can select approvedGeneSymbol,
 omimID, description, omimPhenotypeMapKey, and inhMode. </li>
 <li>Click on the <button>get output</button> will bring you to the results page:
 <pre>chr1	11166591	11322608	MTOR	601231,	Smith-Kingsmore syndrome,Focal cortical dysplasia, type II, somatic,	3,	Autosomal dominant</pre></li></ol>
 <p>For a quick link to pre-fill these options, click 
 <a href="http://genome.ucsc.edu/cgi-bin/hgTables?hgS_doOtherUser=submit&hgS_otherUserName=dschmelt&hgS_otherUserSessionName=omimPhenotypeTableBrowserEx19">
 this session link</a>.