| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42605132-42605386 | Common:2; Rare:49 | ||||
| chr15:42736297-42736541 | Common:3; Rare:101; Clinvar (benign):4 | ||||
| chr15:43240278-43240334 | Rare:14 | ||||
| chr15:43249720-43249897 | Common:1; Rare:31 | ||||
| chr15:43249920-43250039 | Common:1; Rare:16 | ||||
| chr15:43253552-43253628 | Rare:28 | ||||
| chr15:43329977-43330079 | Common:1; Rare:46 | ||||
| chr15:43788665-43788820 | Common:1; Rare:26 | ||||
| chr15:44287918-44288050 | Rare:25 | ||||
| chr15:44489574-44489775 | Common:1; Rare:36 | ||||
| chr15:44535830-44536153 | Common:1; Rare:55 | ||||
| chr15:44537835-44537850 | Rare:2 | ||||
| chr15:44662572-44662803 | Common:1; Rare:46 | ||||
| chr15:44683352-44683498 | Rare:27 | ||||
| chr15:44710301-44710456 | Rare:22 |