6254a2f3273acb0889ba875ffab273f0099cea16
galt
  Tue May 21 00:17:23 2019 -0700
Fixe problems found by htmlCheck validate and hgNearTest robot

diff --git src/hg/makeDb/trackDb/human/snp150Common.html src/hg/makeDb/trackDb/human/snp150Common.html
index cde8a48..bc554a7 100644
--- src/hg/makeDb/trackDb/human/snp150Common.html
+++ src/hg/makeDb/trackDb/human/snp150Common.html
@@ -27,30 +27,30 @@
 that include a "COMMON" flag in the INFO column.  That is determined by a different method,
 and is generally a superset of the UCSC Common set.
 dbSNP uses frequency data from the
 <a href="http://www.internationalgenome.org/" target=_blank>1000 Genomes Project</a>
 only, and considers a variant COMMON if it has a MAF of at least 0.01 in any of the five
 super-populations:
 <ul>
   <li>African (AFR)</li>
   <li>Admixed American (AMR)</li>
   <li>East Asian (EAS)</li>
   <li>European (EUR)</li>
   <li>South Asian (SAS)</li>
 </ul>
 In build 151 (which has replaced build 150 on the dbSNP web and download site),
 dbSNP marks approximately 38M variants as COMMON; 23M of those have a
-global MAF < 0.01.  The remainder should be in agreement with UCSC's Common subset.
+global MAF &lt; 0.01.  The remainder should be in agreement with UCSC's Common subset.
 </p>
 <P>
 The selection of SNPs with a minor allele frequency of 1% or greater
 is an attempt to identify variants that appear to be reasonably common
 in the general population.  Taken as a set, common variants should be
 less likely to be associated with severe genetic diseases due to the
 effects of natural selection,
 following the view that deleterious variants are not likely to become
 common in the population.
 However, the significance of any particular variant should be interpreted
 only by a trained medical geneticist using all available information.
 </P>
 
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