| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:75842992-75843673 | Common:1; Rare:240 | ||||
| chr15:75843696-75844085 | Common:1; Rare:132 | ||||
| chr15:75844098-75844257 | Common:1; Rare:60 | ||||
| chr15:75844412-75844541 | Common:4; Rare:42 | ||||
| chr15:75903530-75903635 | Common:2; Rare:20 | ||||
| chr15:75903714-75904075 | Rare:144 | ||||
| chr15:75904324-75904603 | Common:2; Rare:74 | ||||
| chr15:76310822-76311055 | Common:4; Rare:44 | ||||
| chr15:76311328-76311699 | Common:2; Rare:123; Clinvar:7; Clinvar (benign):9 | ||||
| chr15:76904711-76904844 | Rare:28 | ||||
| chr15:76904945-76905168 | Rare:37 | ||||
| chr15:76905204-76905531 | Common:3; Rare:105 | ||||
| chr15:76931471-76932012 | Common:2; Rare:157 | ||||
| chr15:76994080-76994242 | Common:2; Rare:36 | ||||
| chr15:76995073-76995140 | Rare:21; Clinvar (benign):1 |