| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:28886069-28886219 | Common:1; Rare:48 | ||||
| chr15:28886334-28886734 | Common:4; Rare:133 | ||||
| chr15:29269732-29269939 | Common:2; Rare:103 | ||||
| chr15:29821453-29821661 | Rare:52 | ||||
| chr15:29821727-29822015 | Common:2; Rare:134 | ||||
| chr15:29822422-29822677 | Common:2; Rare:108 | ||||
| chr15:30625950-30626180 | Common:4; Rare:63 | ||||
| chr15:30626296-30626815 | Common:2; Rare:145 | ||||
| chr15:30903610-30903954 | Common:3; Rare:89 | ||||
| chr15:30904261-30904661 | Common:2; Rare:165 | ||||
| chr15:30921978-30922378 | Common:6; Rare:147; Clinvar (pathogenic):2 | ||||
| chr15:30991537-30991799 | Common:4; Rare:93 | ||||
| chr15:30991869-30992028 | Common:1; Rare:66 | ||||
| chr15:30992062-30992226 | Common:1; Rare:31 | ||||
| chr15:31326394-31326752 | Common:3; Rare:169 |