| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:29968866-29969187 | Common:3; Rare:111 | ||||
| chr15:30903777-30903943 | Rare:43 | ||||
| chr15:32615112-32615643 | Common:7; Rare:133 | ||||
| chr15:32641576-32641778 | Common:2; Rare:51 | ||||
| chr15:34101835-34102083 | Common:1; Rare:52 | ||||
| chr15:34224954-34225135 | Rare:69 | ||||
| chr15:34343075-34343234 | Common:4; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:34367163-34367320 | Common:1; Rare:64 | ||||
| chr15:34583620-34583730 | Common:1; Rare:37 | ||||
| chr15:34588444-34588542 | Rare:31 | ||||
| chr15:34988193-34988409 | Common:2; Rare:89 | ||||
| chr15:35546137-35546252 | Common:1; Rare:42 | ||||
| chr15:37100366-37100775 | Common:1; Rare:130 | ||||
| chr15:37101264-37101411 | Common:23; Rare:62 | ||||
| chr15:39580873-39581083 | Rare:58 |