| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:58749482-58749860 | Common:2; Rare:126 | ||||
| chr15:58770910-58771327 | Common:5; Rare:157 | ||||
| chr15:58771825-58772114 | Common:1; Rare:127 | ||||
| chr15:59372566-59372692 | Common:1; Rare:33 | ||||
| chr15:59372816-59373021 | Common:1; Rare:66 | ||||
| chr15:59680242-59680407 | Common:1; Rare:54 | ||||
| chr15:60479095-60479209 | Common:1; Rare:41 | ||||
| chr15:62390448-62390576 | Rare:56 | ||||
| chr15:63042605-63042938 | Rare:102; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:63048682-63048707 | Rare:4 | ||||
| chr15:63049254-63049426 | Common:1; Rare:44 | ||||
| chr15:63063838-63064109 | Common:1; Rare:67; Clinvar:3; Clinvar (benign):3 | ||||
| chr15:63121702-63121889 | Common:1; Rare:55 | ||||
| chr15:63122389-63122662 | Common:4; Rare:91 | ||||
| chr15:63157126-63157557 | Common:3; Rare:129 |