| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:112379786-112380187 | Common:4; Rare:152 | ||||
| chr9:113150940-113151036 | Rare:35 | ||||
| chr9:113221247-113221619 | Common:1; Rare:116 | ||||
| chr9:113275371-113275746 | Common:5; Rare:120; Clinvar (pathogenic):1 | ||||
| chr9:113340237-113340372 | Common:2; Rare:33 | ||||
| chr9:113376914-113377124 | Common:8; Rare:70 | ||||
| chr9:113410317-113410729 | Common:3; Rare:120 | ||||
| chr9:113565377-113565710 | Common:2; Rare:79 | ||||
| chr9:116687221-116687364 | Common:3; Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120580112-120580228 | Rare:35; Clinvar:5 | ||||
| chr9:120793242-120793534 | Common:1; Rare:105 | ||||
| chr9:120842897-120843107 | Common:1; Rare:77 | ||||
| chr9:120929152-120929183 | Rare:9 | ||||
| chr9:121074857-121074977 | Rare:58 | ||||
| chr9:121201832-121202149 | Common:2; Rare:93 |