| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:66868777-66869050 | Common:6; Rare:59 | ||||
| chr15:66905248-66905452 | Common:2; Rare:33 | ||||
| chr15:67067239-67067383 | Rare:26 | ||||
| chr15:67067465-67067944 | Common:3; Rare:90 | ||||
| chr15:67091258-67091578 | Common:1; Rare:76 | ||||
| chr15:67106486-67106593 | Common:2; Rare:17 | ||||
| chr15:67107102-67107300 | Common:3; Rare:35 | ||||
| chr15:67109700-67110002 | Rare:63 | ||||
| chr15:67121070-67121349 | Common:3; Rare:56 | ||||
| chr15:67134255-67134531 | Common:3; Rare:43 | ||||
| chr15:67146958-67147175 | Common:2; Rare:62 | ||||
| chr15:67147724-67147896 | Rare:30 | ||||
| chr15:67150184-67150394 | Common:3; Rare:46 | ||||
| chr15:67165022-67165315 | Common:2; Rare:80; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr15:67170400-67170605 | Rare:46; Clinvar:1; Clinvar (benign):2 |