| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:63053066-63053294 | Rare:48 | ||||
| chr15:64162087-64162430 | Rare:85 | ||||
| chr15:64884075-64884119 | Common:2; Rare:4 | ||||
| chr15:64955011-64955222 | Common:4; Rare:45 | ||||
| chr15:64965388-64965516 | Rare:34; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:65304386-65304679 | Common:5; Rare:132 | ||||
| chr15:67059180-67059441 | Rare:44 | ||||
| chr15:67107016-67107283 | Common:2; Rare:58 | ||||
| chr15:67179656-67179867 | Common:2; Rare:37 | ||||
| chr15:68819421-68819481 | Rare:13 | ||||
| chr15:71341737-71342040 | Rare:69 | ||||
| chr15:72473765-72473823 | Rare:13 | ||||
| chr15:73689346-73689469 | Common:3; Rare:19 | ||||
| chr15:73927695-73927816 | Common:1; Rare:38 | ||||
| chr15:75716280-75716536 | Rare:30 |