| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:63053695-63053989 | Common:3; Rare:56 | ||||
| chr15:63062210-63062872 | Common:2; Rare:183; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr15:63063774-63063855 | Rare:14 | ||||
| chr15:63121674-63121879 | Rare:60 | ||||
| chr15:63122362-63122662 | Common:4; Rare:98 | ||||
| chr15:63156413-63156758 | Common:1; Rare:86 | ||||
| chr15:63157099-63157249 | Rare:27 | ||||
| chr15:63157386-63157573 | Common:2; Rare:82 | ||||
| chr15:63189228-63189736 | Common:3; Rare:147 | ||||
| chr15:63189984-63190090 | Rare:19 | ||||
| chr15:63277387-63277715 | Common:4; Rare:73 | ||||
| chr15:63332139-63332261 | Rare:19 | ||||
| chr15:63381634-63381973 | Common:2; Rare:114 | ||||
| chr15:63504384-63504689 | Common:2; Rare:102 | ||||
| chr15:63544418-63544524 | Common:1; Rare:14 |