| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:58138069-58138502 | Common:2; Rare:79 | ||||
| chr15:58331990-58332297 | Common:4; Rare:54 | ||||
| chr15:58410456-58410579 | Common:1; Rare:25 | ||||
| chr15:58431347-58432018 | Common:6; Rare:149; Clinvar:1 | ||||
| chr15:58770954-58771323 | Common:3; Rare:147 | ||||
| chr15:59372529-59373048 | Common:4; Rare:164 | ||||
| chr15:59689145-59689497 | Common:7; Rare:169 | ||||
| chr15:60479065-60479207 | Common:2; Rare:58 | ||||
| chr15:60592471-60592758 | Common:1; Rare:78 | ||||
| chr15:61229226-61229411 | Common:1; Rare:46 | ||||
| chr15:62060344-62060511 | Rare:69 | ||||
| chr15:62835502-62835767 | Common:1; Rare:82 | ||||
| chr15:63042419-63042487 | Common:1; Rare:22 | ||||
| chr15:63042505-63042913 | Common:4; Rare:127; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:63048335-63048675 | Common:4; Rare:129; Clinvar:5; Clinvar (benign):4 |