| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43517456-43517676 | Common:2; Rare:54 | ||||
| chr15:43746292-43746464 | Common:1; Rare:67 | ||||
| chr15:44195225-44195522 | Common:3; Rare:96 | ||||
| chr15:44288374-44288749 | Common:38; Rare:222 | ||||
| chr15:44536663-44537197 | Common:1; Rare:162 | ||||
| chr15:44711346-44711582 | Rare:69; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45023052-45023260 | Common:3; Rare:55 | ||||
| chr15:45201095-45201155 | Common:1; Rare:30 | ||||
| chr15:45378456-45378579 | Common:2; Rare:36; Clinvar:1; Clinvar (benign):6 | ||||
| chr15:45587281-45587470 | Common:1; Rare:55; Clinvar:6; Clinvar (benign):1 | ||||
| chr15:45587703-45587828 | Common:1; Rare:29 | ||||
| chr15:47184181-47184385 | Common:1; Rare:66 | ||||
| chr15:48178111-48178431 | Common:1; Rare:98 | ||||
| chr15:48330977-48331160 | Common:3; Rare:40 | ||||
| chr15:48331367-48331465 | Rare:32 |