---------------------------------------------------------------


hg19.trackDb.html : Differences exist between hgwbeta and hgw2 

(RR fields taken from public MySql server, not individual machine)

6676,6687d6675
< clinGenComp | <p>
< clinGenComp | Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E
< clinGenComp | <em>et al</em>.
< clinGenComp | <a href="https://linkinghub.elsevier.com/retrieve/pii/S1098-3600(21)03031-8" target="_blank">
< clinGenComp | Standards and guidelines for the interpretation of sequence variants: a joint consensus
< clinGenComp | recommendation of the American College of Medical Genetics and Genomics and the Association for
< clinGenComp | Molecular Pathology</a>.
< clinGenComp | <em>Genet Med</em>. 2015 May;17(5):405-24.
< clinGenComp | PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/25741868" target="_blank">25741868</a>; PMC: <a
< clinGenComp | href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4544753/" target="_blank">PMC4544753</a>
< clinGenComp | </p>
< clinGenComp | 

6708a6697,6707
> clinGenComp | <p>
> clinGenComp | Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E
> clinGenComp | <em>et al</em>.
> clinGenComp | <a href="https://linkinghub.elsevier.com/retrieve/pii/S1098-3600(21)03031-8" target="_blank">
> clinGenComp | Standards and guidelines for the interpretation of sequence variants: a joint consensus
> clinGenComp | recommendation of the American College of Medical Genetics and Genomics and the Association for
> clinGenComp | Molecular Pathology</a>.
> clinGenComp | <em>Genet Med</em>. 2015 May;17(5):405-24.
> clinGenComp | PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/25741868" target="_blank">25741868</a>; PMC: <a
> clinGenComp | href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4544753/" target="_blank">PMC4544753</a>
> clinGenComp | </p>

77991,77994d77989
< wgEncodeGencodeSuper | <p>
< wgEncodeGencodeSuper | <span style="font-weight: bold;">GENCODE version 47lift37 (mapped from GRCh38 to GRCh37)</span>
< wgEncodeGencodeSuper | corresponds to Ensembl 113.
< wgEncodeGencodeSuper | </p>