90555c79f13bedec650b761a878c23a9620001bc
kuhn
  Tue Dec 3 13:20:04 2019 -0800
replaced the word thousand with ,000 so it reads better.  dropped space in rsIDs

diff --git src/hg/makeDb/trackDb/human/dbSnp153Composite.html src/hg/makeDb/trackDb/human/dbSnp153Composite.html
index 8699190..9d80635 100644
--- src/hg/makeDb/trackDb/human/dbSnp153Composite.html
+++ src/hg/makeDb/trackDb/human/dbSnp153Composite.html
@@ -17,59 +17,59 @@
 dbSNP remapped variants from hg38 to hg19 (GRCh37);
 approximately 658 million distinct variants were mapped to
 over 683 million genomic locations
 including alternate haplotype and fix patch sequences (not
 all of which are included in UCSC's hg19).
 </p>
 <p>
 This track includes four subtracks of variants:
   <ul>
     <li><b>All dbSNP (153)</b>: the entire set (683 million for hg19, 702 million for hg38)
     </li>
     <li><b>Common dbSNP (153)</b>: approximately 15 million variants with a minor allele
       frequency (MAF) of at least 1% (0.01) in the 1000 Genomes Phase 3 dataset.
       Variants in the Mult. subset (below) are excluded.
     </li>
-    <li><b>ClinVar dbSNP (153)</b>: approximately 455 thousand variants mentioned in ClinVar.
+    <li><b>ClinVar dbSNP (153)</b>: approximately 455,000 variants mentioned in ClinVar.
       <b>Note:</b> that includes both benign and pathogenic (as well as uncertain) variants.
       Variants in the Mult. subset (below) are excluded.
     </li>
     <li><b>Mult. dbSNP (153)</b>: variants that have been mapped to multiple chromosomes,
       for example chr1 and chr2,
       raising the question of whether the variant is really a variant or just a difference
       between duplicated sequences.
       There are some exceptions in which a variant is mapped to more than one reference
       sequence, but not culled into this set:
       <ul>
         <li>A variant may appear in both X and Y
           pseudo-autosomal regions (PARs) without being included in this set.
         </li>
         <li>A variant may also appear in a main chromosome as well as an alternate haplotype
           or fix patch sequence assigned to that chromosome.
         </li>
       </ul>
     </li>
   </ul>
 </p>
 <p>
 A fifth subtrack highlights coordinate ranges to which dbSNP mapped a variant but with genomic
 coordinates that are not internally consistent, i.e. different coordinate ranges were provided
 when describing different alleles.  This can occur due to a bug with mapping variants from one
 assembly sequence to another when there is an indel difference between the assembly sequences:
   <ul>
-    <li><b>Map Err (153)</b>: around 120 thousand mappings of 55 thousand distinct rs IDs for hg19
-      and 149 thousand mappings of 86 thousand distinct rs IDs for hg38.
+    <li><b>Map Err (153)</b>: around 120,000 mappings of 55,000 distinct rs IDs for hg19
+      and 149,000 mappings of 86,000 distinct rs IDs for hg38.
   </ul>
 </p>
 
 <h2>Interpreting and Configuring the Graphical Display</h2>
 <p>
 SNVs and pure deletions are displayed as boxes covering the affected base(s).
 Pure insertions are drawn as single-pixel tickmarks between
 the base before and the base after the insertion.
 </p><p>
 Insertions and/or deletions in repetitive regions may be represented by a half-height box
 showing uncertainty in placement, followed by a full-height box showing the number of deleted
 bases, or a full-height tickmark to indicate an insertion.
 When an insertion or deletion falls in a repetitive region, the placement may be ambiguous.
 For example, if the reference genome contains "TAAAG" but some
 individuals have "TAAG" at the same location, then the variant is a deletion of a single