f1944b9c04bb45c304c1bfa917141a50b0d2a6d6
dschmelt
  Fri Oct 9 14:41:16 2020 -0700
CR typo fixes #26295

diff --git src/hg/makeDb/trackDb/human/decipher.html src/hg/makeDb/trackDb/human/decipher.html
index 70927ee..7185c60 100644
--- src/hg/makeDb/trackDb/human/decipher.html
+++ src/hg/makeDb/trackDb/human/decipher.html
@@ -43,31 +43,31 @@
 <A HREF="https://decipher.sanger.ac.uk" TARGET=_BLANK>DECIPHER</A>
 database of submicroscopic chromosomal imbalance 
 collects clinical information about chromosomal 
 microdeletions/duplications/insertions, translocations and inversions, 
 and displays this information on the human genome map.
 <p>
 This track shows genomic regions of reported cases and their 
 associated phenotype information.  All data have passed the strict
 consent requirements of the DECIPHER project and are approved for
 unrestricted public release.  Clicking the Patient View ID link
 brings up a more detailed informational page on the patient at the 
 DECIPHER web site. 
 
 <H2>Display Conventions and Configuration</H2>
 <P>
-The genomic locations of DECIPHER variants are labelled with the DECIPHER variant descriptions. 
+The genomic locations of DECIPHER variants are labeled with the DECIPHER variant descriptions. 
 <b>Mouseover</b> on items shows variant details, clinical interpretation, and associated conditions. 
 Further information on each variant is displayed on the details page by a click onto any variant. 
 </p>
 
 <P>
 For the <b>CNVs track</b>, the entries are colored by the <b>type of variant</b>:
 <ul>
  <li><b><font color="red">red</font></b> for loss</li>
  <li><b><font color="blue">blue</font></b> for gain</li>
  <li><b><font color="grey">grey</font></b> for amplification</li>
 </ul>
 </P>
 
 <P>
 A light-to-dark color gradient indicates the <b>clinical significance</b> of each variant, with