59826a66ca3d544754b5d4292155d2ac384019b3
jnavarr5
  Tue Jun 17 16:39:58 2025 -0700
Adding the image of the 'lifted' icon to the text, no Redmine.

diff --git src/hg/makeDb/trackDb/human/revel.html src/hg/makeDb/trackDb/human/revel.html
index a9438fd0f23..7d6d994807d 100644
--- src/hg/makeDb/trackDb/human/revel.html
+++ src/hg/makeDb/trackDb/human/revel.html
@@ -109,31 +109,31 @@
     </tr>
   </tbody>
 </table>
 
 <p>
 More details on these scoring ranges can be found in Bergquist et al. Genet Med 2025, Table 2:
 <img src="../images/bergquist25.png" alt="Table 2 from Bergquist Genet Med 2025">
 </p>
 
 <p>For hg38, note that the data was converted from the hg19 data using the UCSC
 liftOver program, by the REVEL authors. This can lead to missing values or
 duplicated values. When a hg38 position is annotated with two scores due to the
 lifting, the authors removed all the scores for this position. They did the same when
 the reference allele has changed from hg19 to hg38.  Also, on hg38, the track has
 the &quot;lifted&quot; icon to indicate
-this. You can double-check if a nucleotide
+this <img class="gbsInlineImg" src="../images/19.jpg">. You can double-check if a nucleotide
 position is possibly affected by the lifting procedure by activating the track
 &quot;Hg19 Mapping&quot; under &quot;Mapping and Sequencing&quot;.
 </p>
 
 <h2>Data access</h2>
 <p>
 REVEL scores are available at the 
 <a href="https://sites.google.com/site/revelgenomics/" target="_blank">
 REVEL website</a>.  
 The site provides precomputed REVEL scores for all possible human missense variants 
 to facilitate the identification of pathogenic variants among the large number of 
 rare variants discovered in sequencing studies.
 
 </p>