Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:45587558-45587807 | Common:2; Rare:80 | ||||
chr15:45645716-45645903 | Rare:36 | ||||
chr15:48331367-48331465 | Rare:32 | ||||
chr15:48645674-48645929 | Common:2; Rare:85; Clinvar (benign):1 | ||||
chr15:48878034-48878394 | Rare:130 | ||||
chr15:49046371-49046617 | Common:2; Rare:86 | ||||
chr15:49155528-49155845 | Common:2; Rare:108 | ||||
chr15:49170101-49170290 | Rare:41 | ||||
chr15:49423111-49423431 | Common:1; Rare:53 | ||||
chr15:49620810-49621105 | Common:6; Rare:113 | ||||
chr15:50354880-50354998 | Rare:17 | ||||
chr15:50355058-50355504 | Common:3; Rare:174 | ||||
chr15:50424126-50424467 | Common:2; Rare:124 | ||||
chr15:50686713-50686905 | Common:4; Rare:80 | ||||
chr15:50908600-50908766 | Common:1; Rare:68; Clinvar (benign):2 |