Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:23039490-23039812 | Common:1; Rare:130 | ||||
chr15:23565579-23565675 | Rare:24 | ||||
chr15:24954939-24955040 | Rare:62 | ||||
chr15:25438220-25438554 | Common:1; Rare:104; Clinvar (benign):1 | ||||
chr15:25438701-25438758 | Rare:16 | ||||
chr15:25438880-25439477 | Common:6; Rare:210 | ||||
chr15:29269716-29269992 | Common:2; Rare:127 | ||||
chr15:30625642-30625848 | Common:4; Rare:51 | ||||
chr15:30625993-30626148 | Common:3; Rare:38 | ||||
chr15:30903585-30903976 | Common:3; Rare:99 | ||||
chr15:30991113-30991188 | Common:1; Rare:16 | ||||
chr15:30991484-30992055 | Common:6; Rare:213 | ||||
chr15:31031757-31031905 | Common:1; Rare:21 | ||||
chr15:31326035-31327026 | Common:7; Rare:403 | ||||
chr15:31327047-31327216 | Rare:61 |