| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:45129847-45130004 | Rare:34 | ||||
| chr15:45378515-45378678 | Common:3; Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:45587117-45587265 | Rare:27 | ||||
| chr15:45587307-45587450 | Rare:45; Clinvar:6 | ||||
| chr15:45634923-45635084 | Rare:45 | ||||
| chr15:48331367-48331440 | Rare:22 | ||||
| chr15:48645698-48645887 | Common:2; Rare:61; Clinvar (benign):1 | ||||
| chr15:48878038-48878194 | Rare:62 | ||||
| chr15:49046371-49046622 | Common:2; Rare:87 | ||||
| chr15:49155570-49155842 | Common:2; Rare:92 | ||||
| chr15:49620810-49621103 | Common:6; Rare:113 | ||||
| chr15:50355093-50355501 | Common:3; Rare:163 | ||||
| chr15:50686673-50686905 | Common:4; Rare:94 | ||||
| chr15:50765580-50765742 | Common:1; Rare:56 | ||||
| chr15:50908573-50908763 | Common:2; Rare:79; Clinvar (benign):2 |