| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:96070633-96071033 | Common:7; Rare:135 | ||||
| chr15:96170920-96171330 | Common:3; Rare:80 | ||||
| chr15:96200520-96201040 | Common:1; Rare:96 | ||||
| chr15:96209090-96209440 | Common:6; Rare:99 | ||||
| chr15:96209420-96209780 | Common:6; Rare:111 | ||||
| chr15:96326766-96327568 | Common:14; Rare:278 | ||||
| chr15:96328175-96328379 | Common:3; Rare:48 | ||||
| chr15:96329604-96329739 | Common:4; Rare:64 | ||||
| chr15:96331334-96331741 | Common:3; Rare:112 | ||||
| chr15:96333845-96334098 | Rare:67 | ||||
| chr15:96334464-96335015 | Common:2; Rare:239; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr15:96335227-96335675 | Rare:246 | ||||
| chr15:96336345-96336684 | Common:2; Rare:80 | ||||
| chr15:96336638-96337055 | Common:2; Rare:155 | ||||
| chr15:96336999-96337220 | Rare:82 |