| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35072555-35072892 | Rare:82; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35103090-35103303 | Common:1; Rare:69 | ||||
| chr9:35489922-35490139 | Common:2; Rare:61 | ||||
| chr9:35657850-35658376 | Common:8; Rare:439; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35732073-35732334 | Common:2; Rare:70 | ||||
| chr9:35732373-35732683 | Common:3; Rare:78 | ||||
| chr9:35748965-35749395 | Common:2; Rare:157 | ||||
| chr9:35814983-35815294 | Rare:79 | ||||
| chr9:36190715-36190964 | Common:1; Rare:84 | ||||
| chr9:36258386-36258622 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36572749-36572935 | Common:1; Rare:60 | ||||
| chr9:37120153-37120614 | Common:2; Rare:143 | ||||
| chr9:37422617-37422755 | Common:2; Rare:72 | ||||
| chr9:37576267-37576560 | Common:1; Rare:79 | ||||
| chr9:37650705-37651032 | Common:1; Rare:97 |