| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41231039-41231356 | Rare:99 | ||||
| chr15:41231406-41231441 | Rare:12; Clinvar (pathogenic):1 | ||||
| chr15:41332076-41332272 | Common:2; Rare:44 | ||||
| chr15:41332298-41332381 | Rare:42 | ||||
| chr15:41332437-41332998 | Common:2; Rare:232 | ||||
| chr15:41333008-41333251 | Common:1; Rare:61 | ||||
| chr15:41402310-41402593 | Common:4; Rare:105; Clinvar:3; Clinvar (benign):1 | ||||
| chr15:41416725-41417209 | Common:4; Rare:163 | ||||
| chr15:41417440-41417614 | Rare:38 | ||||
| chr15:41477362-41477492 | Common:1; Rare:28 | ||||
| chr15:41493147-41493391 | Rare:55 | ||||
| chr15:41493517-41493930 | Rare:113 | ||||
| chr15:41494288-41494638 | Common:1; Rare:75 | ||||
| chr15:41543992-41544037 | Common:1; Rare:10 | ||||
| chr15:41544066-41544379 | Common:1; Rare:102 |