| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42491016-42491196 | Common:1; Rare:59 | ||||
| chr15:42548725-42548868 | Common:2; Rare:78 | ||||
| chr15:43106021-43106218 | Rare:62 | ||||
| chr15:43330543-43330736 | Common:1; Rare:71 | ||||
| chr15:43370849-43371090 | Common:3; Rare:56 | ||||
| chr15:43510688-43510954 | Rare:85 | ||||
| chr15:43746285-43746465 | Common:1; Rare:69 | ||||
| chr15:44536863-44537386 | Common:3; Rare:195 | ||||
| chr15:44711341-44711612 | Rare:84; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45201111-45201151 | Common:1; Rare:18 | ||||
| chr15:45587093-45587450 | Common:1; Rare:88; Clinvar:6; Clinvar (benign):1 | ||||
| chr15:48331383-48331454 | Rare:23 | ||||
| chr15:48645663-48645873 | Common:2; Rare:68; Clinvar (benign):1 | ||||
| chr15:49155558-49155832 | Common:2; Rare:94 | ||||
| chr15:49423111-49423431 | Common:1; Rare:53 |