| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35812131-35812302 | Rare:67 | ||||
| chr9:35814963-35815344 | Common:1; Rare:95 | ||||
| chr9:35815435-35815577 | Common:1; Rare:33 | ||||
| chr9:35829048-35829293 | Common:2; Rare:63 | ||||
| chr9:36036695-36036986 | Common:3; Rare:83 | ||||
| chr9:36190725-36191024 | Common:2; Rare:97 | ||||
| chr9:36258348-36258639 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36400251-36400592 | Common:3; Rare:101 | ||||
| chr9:36400753-36401008 | Common:3; Rare:99 | ||||
| chr9:36401136-36401248 | Common:1; Rare:38 | ||||
| chr9:37120187-37120646 | Common:2; Rare:143 | ||||
| chr9:37422576-37422747 | Common:2; Rare:89 | ||||
| chr9:37464955-37465041 | Common:1; Rare:26 | ||||
| chr9:37465073-37465156 | Common:1; Rare:28 | ||||
| chr9:37465775-37466026 | Common:3; Rare:59 |