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/encodeYaleChIPSTAT1Sites.html src/hg/makeDb/trackDb/human/encodeYaleChIPSTAT1Sites.html
index a2e6056..e62efc0 100644
--- src/hg/makeDb/trackDb/human/encodeYaleChIPSTAT1Sites.html
+++ src/hg/makeDb/trackDb/human/encodeYaleChIPSTAT1Sites.html
@@ -1,29 +1,29 @@
 <H2>Description</H2>
 <P>
 Each of these four tracks shows the binding sites 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: 50mer oligonucleotides tiled every 
 38 bps (overlapping by 12 nts)
 <LI>Maskless design #2: 36mer oligonucleotides tiled end to end
 <LI>Maskless design #3: 50mer 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. See NCBI GEO 
 <A HREF="https://www.ncbi.nlm.nih.gov/projects/geo/query/acc.cgi?acc=
 GSE2714"
 TARGET=_blank>GSE2714</A> for details of the experimental protocols.</P>
 
 <H2>Methods</H2>