1dee540669a2ac51afa2ebdff3b53e7f3abc7cc2
jnavarr5
  Fri Sep 19 12:24:43 2025 -0700
Updating the descripiton to match the styling of the other tracks in the composite, refs #35054

diff --git src/hg/makeDb/trackDb/human/decipherContainer.html src/hg/makeDb/trackDb/human/decipherContainer.html
index 2e2e381dfee..10a0bbc5ce5 100644
--- src/hg/makeDb/trackDb/human/decipherContainer.html
+++ src/hg/makeDb/trackDb/human/decipherContainer.html
@@ -113,62 +113,53 @@
 about the data:
 </P>
 <ul>
   <li><strong>Position:</strong> Specifies the chromosomal range of the CNV.</li>
   <li><strong>Type of CNV:</strong> Indicates if the variation is a loss, gain, or
       deletions/duplications(del/dup).</li>
   <li><strong>Frequency of CNV:</strong> Reflects how often the CNV occurs in the sampled
       population.</li>
   <li><strong>Number of Observations:</strong> The count of times this CNV was observed in the
       dataset.</li>
   <li><strong>Sample Size of Study:</strong> The total number of samples examined.</li>
 </ul>
 
 
 <p>
-For the <b>DDG2P track</b>, items are colored according confidence of gene disease association is true:</p>
+For the <b>DDG2P track</b>, items are colored according to the likelihood that the gene-disease
+association is true:</p>
 <ul>
-    <li style="color: green;">Definitive</li>
-    <li style="color: blue;">Strong</li>
-    <li style="color: orange;">Moderate</li>
-    <li style="color: red;">Limited</li>
-    <li style="color: gray;">Refuted</li>
+    <li> <font style="color: green;"><b>Green</b></font> - Definitive</li>
+    <li> <font style="color: blue;"><b>Blue</b></font> - Strong</li>
+    <li> <font style="color: orange;"><b>Orange</b></font> - Moderate</li>
+    <li> <font style="color: red;"><b>Red</b></font> - Limited</li>
+    <li> <font style="color: gray;"><b>Gray</b></font> - Refuted</li>
 </ul>
 
-<p>Each mouse over item includes the following fields:</p>
-<dl>
-  <dt><strong>G2P ID</strong></dt>
-  <dd>Unique identifier assigned by the Gene2Phenotype (G2P) database.</dd>
-
-  <dt><strong>Number of PubMed IDs</strong></dt>
-  <dd>Count of publications associated with the variant.</dd>
-
-  <dt><strong>Molecular Mechanism</strong></dt>
-  <dd>Description of the molecular processes and interactions causing pathogenic effects.</dd>
-
-  <dt><strong>Allelic Requirements</strong></dt>
-  <dd>Number of alleles required at a locus to produce a pathogenic phenotype (e.g., monoallelic, biallelic).</dd>
-
-  <dt><strong>Variant Consequence</strong></dt>
-  <dd>Predicted effect each allele of a variant has on a transcript.</dd>
-
-  <dt><strong>Disease Name</strong></dt>
-  <dd>Name of the disease associated with the variant.</dd>
-
-  <dt><strong>Date of Last Review</strong></dt>
-  <dd>Most recent date the entry was manually reviewed.</dd>
-</dl>
+<p>Each <b>mouseover</b> tooltip provides the following information:</p>
+<ul>
+  <li><strong>G2P ID</strong>: Unique identifier assigned by the Gene2Phenotype (G2P) database.</li>
+  <li><strong>Number of PubMed IDs</strong>: Count of publications associated with the variant.</li>
+  <li><strong>Molecular Mechanism</strong>: Description of the molecular processes and interactions
+      causing pathogenic effects.</li>
+  <li><strong>Allelic Requirements</strong>: Number of alleles required at a locus to produce a
+      pathogenic phenotype (e.g., monoallelic, biallelic).</li>
+  <li><strong>Variant Consequence</strong>: Predicted effect each allele of a variant has on a
+      transcript.</li>
+  <li><strong>Disease Name</strong>: Name of the disease associated with the variant.</li>
+  <li><strong>Date of Last Review</strong>: Most recent date the entry was manually reviewed.</li>
+</ul>
 
 
 <H2>Method</H2>
 <P>
 Data provided by the DECIPHER project group are imported and processed
 to create a simple BED track to annotate the genomic regions associated
 with individual patients.
 </p>
 <p>
 Data provided by the Gene2Phenotype project group were imported and processed to create a BED-based track
 annotating genomic regions associated with individual patients. Standard genome assembly coordinates
 and gene annotations were used to map DDG2P entries to the browser.
 </P>