| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:116153100-116153826 | Common:3; Rare:218 | ||||
| chr9:116154062-116154239 | Common:1; Rare:51 | ||||
| chr9:116687133-116687370 | Common:7; Rare:149; Clinvar:4; Clinvar (benign):4 | ||||
| chr9:120532500-120532730 | Rare:81 | ||||
| chr9:120580012-120580421 | Common:2; Rare:207; Clinvar:10 | ||||
| chr9:120714333-120714732 | Common:6; Rare:239 | ||||
| chr9:120793227-120793578 | Common:8; Rare:241 | ||||
| chr9:120842875-120843262 | Common:2; Rare:244 | ||||
| chr9:120876360-120876585 | Common:2; Rare:64 | ||||
| chr9:120877089-120877532 | Common:6; Rare:278 | ||||
| chr9:121074811-121074977 | Rare:150 | ||||
| chr9:121075030-121075420 | Rare:126 | ||||
| chr9:121121662-121121770 | Rare:23 | ||||
| chr9:121121672-121121852 | Rare:49 | ||||
| chr9:121201057-121201463 | Common:1; Rare:153 |