| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:110256410-110256725 | Common:5; Rare:109 | ||||
| chr9:110256862-110257097 | Rare:47 | ||||
| chr9:111484138-111484479 | Common:1; Rare:170 | ||||
| chr9:111599367-111599897 | Common:4; Rare:136 | ||||
| chr9:111631065-111631527 | Common:4; Rare:133 | ||||
| chr9:111661486-111661708 | Common:3; Rare:63 | ||||
| chr9:111896642-111896789 | Common:3; Rare:59 | ||||
| chr9:112333473-112333968 | Common:1; Rare:144 | ||||
| chr9:112379765-112380157 | Common:4; Rare:148 | ||||
| chr9:112717985-112718159 | Common:2; Rare:41 | ||||
| chr9:113150641-113151003 | Common:5; Rare:76 | ||||
| chr9:113221221-113221658 | Common:1; Rare:136 | ||||
| chr9:113275159-113275334 | Rare:49 | ||||
| chr9:113275359-113275739 | Common:5; Rare:121; Clinvar (pathogenic):1 | ||||
| chr9:113340237-113340431 | Common:3; Rare:49 |