be3c30eebd8be34d5bf3c382527540fdb280eac9
kuhn
  Fri May 13 14:18:10 2011 -0700
moved table of SNP info off left margin
diff --git src/hg/htdocs/indexNews.html src/hg/htdocs/indexNews.html
index 379727a..3a740d7 100644
--- src/hg/htdocs/indexNews.html
+++ src/hg/htdocs/indexNews.html
@@ -100,57 +100,59 @@
 
                     <li>Flagged SNPs (132): uniquely mapped variants, excluding Common
                     SNPs, that have been flagged by dbSNP as &quot;clinically associated&quot;</li>
 
                     <li>Mult. SNPs (132): variants that have been mapped to more than one
                     genomic location</li>
                     </ul>
                     <P>
                     By default, only the Common SNPs (132) are visible; other tracks must
                     be made visible using the track controls.
                     </P>
                     <P>
                     The counts of distinct reference SNPs and their mappings to hg19
                     differ greatly among the tracks:
                     </P>
+                   <BLOCKQUOTE>
                     <table border="1" cellpadding="3">
                       <tr>
                         <th>Track</th>
                         <th>Reference SNPs</th>
                         <th>Mappings to hg19</th>
                       </tr>
                       <tr>
                         <td>Common SNPs (132)</td>
                         <td>13,842,381</td>
                         <td>14,024,295 *</td>
                       </tr>
                       <tr>
                         <td>Flagged SNPs (132)</td>
                         <td>17,899</td>
                         <td>18,084 *</td>
                       </tr>
                       <tr>
                         <td>Mult. SNPs (132)</td>
                         <td>1,114,599</td>
                         <td>3,568,988</td>
                       </tr>
                       <tr>
                         <td>All SNPs (132)</td>
                         <td>30,030,754</td>
                         <td>33,026,121</td>
                       </tr>
                     </table>
+                   </BLOCKQUOTE>
                     <P>
 
                     * The Common and Flagged tracks have more mappings than SNPs due to the
                     alternate haplotype sequences and the pseudoautosomal regions on X and Y.
                     SNPs are considered uniquely mapped if they map only once to a haploid
                     reference genome.  These regions add non-haploid sequence to the reference
                     genome; therefore, multiple mappings involving these regions are still 
                     considered unique.
 		    </P>
                     <P>
                     You will find the four SNPs (132) tracks on the Human Feb. 2009
                     (GRCh37/hg19) browser in the &quot;Variation and Repeats&quot; group.
 		    </P>
                     <P>
                     Many thanks to dbSNP at NCBI for the data, and to