| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:49170051-49170315 | Rare:58 | ||||
| chr15:49423107-49423362 | Common:1; Rare:43 | ||||
| chr15:49620810-49621134 | Common:7; Rare:124 | ||||
| chr15:50113284-50113498 | Common:1; Rare:38 | ||||
| chr15:50119220-50119384 | Rare:24 | ||||
| chr15:50354877-50355015 | Rare:25 | ||||
| chr15:50355058-50355509 | Common:3; Rare:177 | ||||
| chr15:50424138-50424466 | Common:2; Rare:119 | ||||
| chr15:50686658-50686937 | Common:5; Rare:111 | ||||
| chr15:50765529-50765766 | Common:2; Rare:83 | ||||
| chr15:50908579-50908765 | Common:2; Rare:79; Clinvar (benign):2 | ||||
| chr15:51622570-51622575 | Rare:2 | ||||
| chr15:51622597-51622875 | Rare:93 | ||||
| chr15:51622909-51623071 | Common:3; Rare:57 | ||||
| chr15:51751471-51751707 | Common:1; Rare:58 |