| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41115839-41116306 | Common:2; Rare:131 | ||||
| chr15:41116360-41116797 | Common:1; Rare:133 | ||||
| chr15:41230731-41230876 | Rare:43 | ||||
| chr15:41231053-41231280 | Rare:65 | ||||
| chr15:41231398-41231452 | Rare:17; Clinvar (pathogenic):1 | ||||
| chr15:41332214-41332252 | Rare:12 | ||||
| chr15:41332290-41332404 | Common:1; Rare:53 | ||||
| chr15:41332439-41333057 | Common:2; Rare:248 | ||||
| chr15:41333085-41333254 | Common:1; Rare:30 | ||||
| chr15:41402333-41402643 | Common:4; Rare:104; Clinvar:3; Clinvar (benign):1 | ||||
| chr15:41416742-41417216 | Common:4; Rare:164 | ||||
| chr15:41477359-41477457 | Common:1; Rare:27 | ||||
| chr15:41493092-41493367 | Rare:61 | ||||
| chr15:41493693-41493882 | Rare:61 | ||||
| chr15:41501519-41501708 | Rare:66 |