c613ca6dd305b556af1148511ecd737317b3fe5b
max
  Tue Jun 17 08:48:49 2025 -0700
improving docs page of deleteriousness supertrack, no redmine, email from Heidi Rehm

diff --git src/hg/makeDb/trackDb/human/revel.html src/hg/makeDb/trackDb/human/revel.html
index b1f5e14851b..7df62e53547 100644
--- src/hg/makeDb/trackDb/human/revel.html
+++ src/hg/makeDb/trackDb/human/revel.html
@@ -172,27 +172,25 @@
 <p>
 Thanks to the REVEL development team for providing precomputed data and fixing duplicated values in the hg38 files.
 </p>
 
 <h2>References</h2>
 <p>
 Ioannidis NM, Rothstein JH, Pejaver V, Middha S, McDonnell SK, Baheti S, 
 Musolf A, Li Q, Holzinger E, Karyadi D, et al.
 <a href="https://doi.org/10.1016/j.ajhg.2016.08.016" target = _blank">
 REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants</a>
 <em>Am J Hum Genet</em>. 2016 Oct 6;99(4):877-885.
 PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/27666373" target="_blank">27666373</a>;
 PMC: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5065685/" target="_blank">PMC5065685</a>
 </p>
 
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 <p>
 Bergquist T, Stenton SL, Nadeau EAW, Byrne AB, Greenblatt MS, Harrison SM, Tavtigian SV,
 O&#x27;Donnell-Luria A, Biesecker LG, Radivojac P <em>et al</em>.
 <a href="https://linkinghub.elsevier.com/retrieve/pii/S1098-3600(25)00049-8" target="_blank">
 Calibration of additional computational tools expands ClinGen recommendation options for variant
 classification with PP3/BP4 criteria</a>.
 <em>Genet Med</em>. 2025 Mar 10;27(6):101402.
 PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/40084623" target="_blank">40084623</a>
 </p>