8a144988470f693d6618c13ba5fe364b56b428d2
dschmelt
  Fri Oct 9 14:36:38 2020 -0700
Correcting relative links for #25207

diff --git src/hg/makeDb/trackDb/human/decipher.html src/hg/makeDb/trackDb/human/decipher.html
index 3b1c9c4..70927ee 100644
--- src/hg/makeDb/trackDb/human/decipher.html
+++ src/hg/makeDb/trackDb/human/decipher.html
@@ -60,31 +60,31 @@
 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 
 the lightest shade being benign, to the darkest shade being pathogenic. Detailed information on the 
-CNV color code is described <a href="https://genome.ucsc.edu/goldenPath/help/hgCnvColoring.html">here</a>.
+CNV color code is described <a href="../../goldenPath/help/hgCnvColoring.html">here</a>.
 Items can be filtered according to the size of the variant, variant type, and clinical significance 
 using the track <b>Configure</b> options.
 </P>
  
 <P>
 For the <b>SNVs track</b>, the entries are colored according to the estimated <b>clinical significance</b> 
 of the variant:
 <ul>
  <li><b><font color="black">black</font></b> for likely or definitely pathogenic</li>
  <li><b><font color="#888">dark grey</font></b> for uncertain or unknown</li>
  <li><b><font color="#c8c8c8">light grey</font></b> for likely or definitely benign</li>
  </ul>
 </P>
 
 <H2>Method</H2>