| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35812113-35812326 | Rare:80 | ||||
| chr9:35814980-35815303 | Rare:82 | ||||
| chr9:35815398-35815628 | Common:2; Rare:52 | ||||
| chr9:35828644-35828893 | Common:1; Rare:52 | ||||
| chr9:35829072-35829291 | Common:1; Rare:57 | ||||
| chr9:36036717-36036995 | Common:3; Rare:86 | ||||
| chr9:36037128-36037409 | Common:1; Rare:73 | ||||
| chr9:36136564-36136794 | Common:4; Rare:65 | ||||
| chr9:36190593-36190976 | Common:1; Rare:112 | ||||
| chr9:36258360-36258666 | Common:2; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36400110-36400640 | Common:5; Rare:163 | ||||
| chr9:36400820-36401018 | Common:3; Rare:82 | ||||
| chr9:36401110-36401520 | Common:4; Rare:114 | ||||
| chr9:36487607-36488060 | Common:2; Rare:182 | ||||
| chr9:36572728-36573043 | Common:2; Rare:86 |