| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35689702-35690120 | Common:4; Rare:129; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35691064-35691212 | Common:1; Rare:30 | ||||
| chr9:35698811-35699109 | Common:1; Rare:84 | ||||
| chr9:35731983-35732320 | Common:1; Rare:85 | ||||
| chr9:35732365-35732751 | Common:3; Rare:100 | ||||
| chr9:35748922-35749369 | Common:3; Rare:155 | ||||
| chr9:35812242-35812297 | Rare:22 | ||||
| chr9:35814972-35815293 | Rare:80 | ||||
| chr9:35905897-35906269 | Common:3; Rare:87 | ||||
| chr9:36136621-36136779 | Common:2; Rare:52 | ||||
| chr9:36190715-36191129 | Common:2; Rare:137 | ||||
| chr9:36191142-36191272 | Common:1; Rare:32 | ||||
| chr9:36258353-36258639 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36400841-36401009 | Common:3; Rare:74 | ||||
| chr9:37120144-37120618 | Common:2; Rare:144 |