| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44195262-44195444 | Common:2; Rare:55 | ||||
| chr15:44288224-44288357 | Rare:22 | ||||
| chr15:44288394-44288790 | Common:39; Rare:230 | ||||
| chr15:44427559-44427723 | Common:1; Rare:46 | ||||
| chr15:44536361-44536653 | Common:1; Rare:60 | ||||
| chr15:44536663-44536723 | Rare:11 | ||||
| chr15:44536855-44537425 | Common:3; Rare:204 | ||||
| chr15:44711314-44711612 | Rare:89; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711856-44712020 | Rare:32 | ||||
| chr15:45023052-45023334 | Common:3; Rare:85 | ||||
| chr15:45114170-45114326 | Common:2; Rare:28 | ||||
| chr15:45114502-45114588 | Common:1; Rare:26 | ||||
| chr15:45129862-45130013 | Rare:34 | ||||
| chr15:45200489-45200656 | Common:1; Rare:47 | ||||
| chr15:45201102-45201150 | Common:1; Rare:23 |