| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41115988-41116247 | Common:2; Rare:73 | ||||
| chr15:41416990-41417166 | Common:2; Rare:77 | ||||
| chr15:41827909-41828184 | Common:4; Rare:104 | ||||
| chr15:42273097-42273224 | Common:1; Rare:51 | ||||
| chr15:42273391-42273633 | Rare:88 | ||||
| chr15:42548695-42548868 | Common:3; Rare:88 | ||||
| chr15:43330543-43330708 | Rare:63 | ||||
| chr15:43371030-43371117 | Rare:20 | ||||
| chr15:43746247-43746699 | Common:2; Rare:181 | ||||
| chr15:43776911-43777121 | Common:1; Rare:67 | ||||
| chr15:43824623-43824791 | Common:2; Rare:44 | ||||
| chr15:44536855-44537227 | Common:3; Rare:138 | ||||
| chr15:44711331-44711611 | Rare:85; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45023090-45023334 | Common:1; Rare:75 | ||||
| chr15:45129822-45130013 | Rare:42 |