| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111599623-111599859 | Common:1; Rare:64 | ||||
| chr9:111661486-111661708 | Common:3; Rare:63 | ||||
| chr9:112333601-112333941 | Rare:104 | ||||
| chr9:112379827-112380138 | Common:3; Rare:124 | ||||
| chr9:113056634-113056848 | Common:1; Rare:75; Clinvar:1 | ||||
| chr9:113150680-113151040 | Common:3; Rare:86 | ||||
| chr9:113221257-113221617 | Common:1; Rare:112 | ||||
| chr9:113275354-113275757 | Common:5; Rare:134; Clinvar (pathogenic):1 | ||||
| chr9:113410226-113410734 | Common:3; Rare:153 | ||||
| chr9:113564842-113565145 | Common:4; Rare:64 | ||||
| chr9:114505506-114505666 | Common:1; Rare:39 | ||||
| chr9:114587551-114587901 | Common:3; Rare:139 | ||||
| chr9:115118023-115118389 | Common:3; Rare:95 | ||||
| chr9:115118518-115118864 | Common:2; Rare:58 | ||||
| chr9:116687171-116687364 | Common:4; Rare:74; Clinvar:2; Clinvar (benign):1 |