| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:34337763-34337819 | Rare:20 | ||||
| chr15:34343086-34343273 | Common:4; Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:34367090-34367928 | Common:3; Rare:234 | ||||
| chr15:34437005-34437207 | Common:1; Rare:66 | ||||
| chr15:34437756-34437910 | Common:6; Rare:37 | ||||
| chr15:34582800-34583128 | Common:5; Rare:105 | ||||
| chr15:34583603-34583797 | Common:5; Rare:74 | ||||
| chr15:34588435-34588561 | Rare:36 | ||||
| chr15:34969611-34969974 | Common:6; Rare:103 | ||||
| chr15:34987789-34988072 | Common:3; Rare:59 | ||||
| chr15:34988146-34988461 | Common:3; Rare:116 | ||||
| chr15:34988659-34988819 | Rare:37 | ||||
| chr15:35545909-35546529 | Common:2; Rare:204 | ||||
| chr15:36579217-36579800 | Common:8; Rare:152 | ||||
| chr15:37100315-37100777 | Common:1; Rare:135 |