| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:30991510-30991715 | Common:4; Rare:75 | ||||
| chr15:31326766-31326887 | Rare:46 | ||||
| chr15:32030359-32030521 | Common:6; Rare:44 | ||||
| chr15:32615090-32615150 | Common:1; Rare:18 | ||||
| chr15:32615397-32615534 | Common:3; Rare:36 | ||||
| chr15:33194707-33194963 | Common:1; Rare:73 | ||||
| chr15:34039041-34039348 | Common:4; Rare:93 | ||||
| chr15:34101829-34102144 | Common:1; Rare:67 | ||||
| chr15:34154815-34154988 | Common:3; Rare:36 | ||||
| chr15:34224952-34225200 | Rare:86 | ||||
| chr15:34337960-34338119 | Rare:61 | ||||
| chr15:34343019-34343063 | Common:1; Rare:17; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:34343065-34343324 | Common:4; Rare:70; Clinvar:3; Clinvar (benign):1 | ||||
| chr15:34362173-34362226 | Rare:14 | ||||
| chr15:34366609-34366851 | Common:1; Rare:38 |