| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:28885841-28886179 | Common:1; Rare:100 | ||||
| chr15:29269791-29269907 | Common:1; Rare:44 | ||||
| chr15:29822024-29822192 | Rare:61 | ||||
| chr15:29822250-29822674 | Common:2; Rare:170 | ||||
| chr15:30903689-30903952 | Common:2; Rare:66 | ||||
| chr15:30991563-30991957 | Common:5; Rare:144 | ||||
| chr15:32615081-32615603 | Common:7; Rare:133 | ||||
| chr15:32615737-32615780 | Rare:11 | ||||
| chr15:34101840-34102140 | Common:1; Rare:61 | ||||
| chr15:34224989-34225152 | Rare:63 | ||||
| chr15:34367140-34367360 | Common:2; Rare:93 | ||||
| chr15:34582851-34582935 | Rare:33 | ||||
| chr15:34583574-34583728 | Common:2; Rare:52 | ||||
| chr15:34588447-34588565 | Rare:35 | ||||
| chr15:34795403-34796030 | Common:4; Rare:141; Clinvar:5; Clinvar (benign):4 |