| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:60479037-60479236 | Common:2; Rare:90 | ||||
| chr15:61229219-61229295 | Rare:12 | ||||
| chr15:62060345-62060509 | Rare:69 | ||||
| chr15:62390468-62390576 | Rare:47 | ||||
| chr15:63042578-63043296 | Common:2; Rare:189; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr15:63048269-63048332 | Rare:24 | ||||
| chr15:63048360-63048712 | Common:4; Rare:124; Clinvar:5; Clinvar (benign):4 | ||||
| chr15:63049276-63049480 | Common:1; Rare:51 | ||||
| chr15:63062869-63063128 | Common:2; Rare:50 | ||||
| chr15:63121670-63121903 | Common:1; Rare:69 | ||||
| chr15:63122381-63122662 | Common:4; Rare:93 | ||||
| chr15:63157074-63157244 | Rare:31 | ||||
| chr15:63157363-63157561 | Common:2; Rare:84 | ||||
| chr15:63157700-63157849 | Common:1; Rare:41 | ||||
| chr15:63158014-63158309 | Common:4; Rare:62 |