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/encodeYaleChIPSTAT1Sig.html src/hg/makeDb/trackDb/human/encodeYaleChIPSTAT1Sig.html
index cf7e136..f35aae4 100644
--- src/hg/makeDb/trackDb/human/encodeYaleChIPSTAT1Sig.html
+++ src/hg/makeDb/trackDb/human/encodeYaleChIPSTAT1Sig.html
@@ -1,30 +1,30 @@
 <H2>Description</H2>
 <P>
 Each of these four tracks shows the map of signal intensity 
 (estimating the fold enrichment [log2 scale] of ChIP DNA vs 
 unstimulated DNA) for STAT1 ChIP-chip using Human Hela S3 cells 
 hybridized to four different array designs/platforms. The first 
 three platforms are custom maskless photolithographic arrays 
 with oligonucleotides tiling most of the non-repetitive DNA 
 sequence of the ENCODE regions: 
 <UL>
 <LI>Maskless design #1: 50-mer oligonucleotides tiled every 
 38 bps (overlapping by 12 nts)
 <LI>Maskless design #2: 36-mer oligonucleotides tiled end to end
 <LI>Maskless design #3: 50-mer oligonucleotides tiled end to end
-</UL></P
+</UL></P>
 <P>
 The fourth array platform is an ENCODE PCR 
 Amplicon array manufactured by Bing Ren's lab at UCSD. </P>
 <P>
 Each track shows the combined results of multiple biological replicates: five 
 for the first maskless array (50-mer every 38 bp), two for the 
 second maskless array (36-mer every 36 bp), three for the third 
 maskless array (50-mer every 50 bp) and six for the PCR Amplicon 
 array. For all arrays, the STAT1 ChIP DNA was labeled with Cy5 and 
 the control DNA was labeled with Cy3.</P>
 <P>
 These data are available at NCBI GEO as 
 <A HREF="https://www.ncbi.nlm.nih.gov/projects/geo/query/acc.cgi?acc=
 GSE2714"
 TARGET=_blank>GSE2714</A>, which also provides additional information about