Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48966277-48966642 | Rare:115; Clinvar (pathogenic):2 | ||||
chr19:51594375-51594608 | Common:2; Rare:58 | ||||
chr19:52942563-52942719 | Common:3; Rare:52 | ||||
chr2:285544-285833 | Rare:45 | ||||
chr2:11345428-11345581 | Rare:33 | ||||
chr2:12715928-12716064 | Common:2; Rare:27 | ||||
chr2:13537865-13537938 | Common:1; Rare:17 | ||||
chr2:20447729-20447832 | Rare:26 | ||||
chr2:20448678-20448833 | Common:1; Rare:32 | ||||
chr2:26193642-26193919 | Rare:81; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
chr2:26696413-26696452 | Rare:8 | ||||
chr2:28394670-28394729 | Rare:11 | ||||
chr2:36544246-36544434 | Common:1; Rare:54 | ||||
chr2:38482200-38482491 | Common:2; Rare:69 | ||||
chr2:43006237-43006534 | Common:5; Rare:77 |