Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:15468959-15469330 | Common:2; Rare:114 | ||||
chr9:15469938-15470224 | Rare:90 | ||||
chr9:16542031-16542130 | Rare:21 | ||||
chr9:16722023-16722258 | Common:1; Rare:46 | ||||
chr9:16726812-16726887 | Common:1; Rare:14 | ||||
chr9:16726923-16726955 | Rare:11 | ||||
chr9:22238033-22238149 | Common:1; Rare:19 | ||||
chr9:25677393-25677692 | Common:3; Rare:124 | ||||
chr9:27528264-27528451 | Common:3; Rare:35 | ||||
chr9:27534146-27534389 | Rare:38 | ||||
chr9:27539869-27540011 | Rare:34 | ||||
chr9:32550829-32551198 | Common:1; Rare:144; Clinvar:2; Clinvar (benign):2 | ||||
chr9:33029641-33029900 | Common:1; Rare:62 | ||||
chr9:33165739-33166017 | Common:1; Rare:58 | ||||
chr9:34241000-34241199 | Rare:42 |