4887b61d286a12e4eea1124c1f7685e9f4137ae6
jnavarr5
  Tue Mar 2 16:07:20 2021 -0800
Removing an extra 'and' in the sentence, refs #18492

diff --git src/hg/makeDb/trackDb/human/caddSuper.html src/hg/makeDb/trackDb/human/caddSuper.html
index 4913960..8de4584 100644
--- src/hg/makeDb/trackDb/human/caddSuper.html
+++ src/hg/makeDb/trackDb/human/caddSuper.html
@@ -5,31 +5,31 @@
 CADD is a tool for scoring the deleteriousness of single nucleotide variants as
 well as insertion/deletions variants in the human genome.</p>
 
 <p>
 Some mutation annotations
 tend to exploit a single information type (e.g. phastCons or phyloP for
 conservation) and/or are restricted in scope (e.g. to missense changes). Thus,
 a broadly applicable metric that objectively weights and integrates diverse
 information is needed.  Combined Annotation Dependent Depletion (CADD) is a
 framework that integrates multiple annotations into one metric by contrasting
 variants that survived natural selection with simulated mutations.
 </p>
 
 <p>
 CADD scores strongly correlate with allelic diversity, pathogenicity of both
-coding and non-coding variants, and experimentally measured regulatory effects,
+coding and non-coding variants, experimentally measured regulatory effects,
 and also highly rank causal variants within individual genome sequences.
 Finally, CADD scores of complex trait-associated variants from genome-wide
 association studies (GWAS) are significantly higher than matched controls and
 correlate with study sample size, likely reflecting the increased accuracy of
 larger GWAS.
 </p>
 
 <h2>Display Conventions and Configuration</h2>
 <p>
 There are six subtracks of this track: four for every possible single nucleotide mutation, 
 one for insertions and one for deletions. All subtracks show the CADD Phred
 score on mouseover.<p>
 
 <p>
 <b>Single nucleotide variants (SNV):</b> For SNVs, at every