| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:110207508-110207647 | Rare:48 | ||||
| chr9:110256418-110256725 | Common:5; Rare:107 | ||||
| chr9:111896649-111896784 | Common:3; Rare:49 | ||||
| chr9:112379841-112380179 | Common:3; Rare:132 | ||||
| chr9:112890836-112890930 | Rare:23 | ||||
| chr9:113187941-113188176 | Common:3; Rare:36 | ||||
| chr9:113221221-113221658 | Common:1; Rare:136 | ||||
| chr9:113275397-113275734 | Common:5; Rare:112; Clinvar (pathogenic):1 | ||||
| chr9:113401242-113401406 | Common:5; Rare:78; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410289-113410705 | Common:3; Rare:123 | ||||
| chr9:116687203-116687364 | Common:3; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120714447-120714732 | Common:2; Rare:97 | ||||
| chr9:120793248-120793542 | Common:2; Rare:109 | ||||
| chr9:120842910-120843259 | Common:1; Rare:112 | ||||
| chr9:121074829-121074969 | Rare:68 |