| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44711346-44711611 | Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44956606-44956793 | Rare:62 | ||||
| chr15:45022796-45023237 | Common:6; Rare:109 | ||||
| chr15:45378321-45378692 | Common:4; Rare:112; Clinvar:3; Clinvar (benign):12 | ||||
| chr15:45402184-45402360 | Common:2; Rare:53 | ||||
| chr15:45417501-45417583 | Rare:16 | ||||
| chr15:45430438-45430701 | Common:1; Rare:66 | ||||
| chr15:45522362-45522918 | Common:1; Rare:157 | ||||
| chr15:45587050-45587263 | Common:1; Rare:41 | ||||
| chr15:45587281-45587470 | Common:1; Rare:55; Clinvar:6; Clinvar (benign):1 | ||||
| chr15:45587553-45587815 | Common:2; Rare:83 | ||||
| chr15:45634710-45635084 | Common:1; Rare:97 | ||||
| chr15:48178085-48178455 | Common:1; Rare:113 | ||||
| chr15:48331019-48331160 | Common:3; Rare:34 | ||||
| chr15:48331383-48331476 | Rare:31 |