| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43826838-43827087 | Rare:99 | ||||
| chr15:44194421-44194653 | Rare:53 | ||||
| chr15:44195194-44195511 | Common:3; Rare:101 | ||||
| chr15:44287879-44288320 | Common:1; Rare:76 | ||||
| chr15:44288324-44288790 | Common:39; Rare:240 | ||||
| chr15:44426847-44427135 | Rare:71 | ||||
| chr15:44427137-44427820 | Common:5; Rare:176 | ||||
| chr15:44427821-44427974 | Rare:42 | ||||
| chr15:44427993-44428231 | Common:1; Rare:61 | ||||
| chr15:44536651-44536934 | Rare:66 | ||||
| chr15:44537007-44537218 | Common:1; Rare:84 | ||||
| chr15:44537667-44537818 | Common:1; Rare:34 | ||||
| chr15:44663057-44663274 | Common:1; Rare:48 | ||||
| chr15:44663546-44663933 | Rare:167; Clinvar:12; Clinvar (benign):6 | ||||
| chr15:44711282-44711675 | Rare:119; Clinvar:1; Clinvar (pathogenic):1 |