| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35072442-35072892 | Rare:105; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35161773-35162178 | Common:4; Rare:113 | ||||
| chr9:35489922-35490121 | Common:1; Rare:56 | ||||
| chr9:35657850-35658371 | Common:8; Rare:437; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35685432-35685789 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr9:35689702-35689969 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35689971-35690042 | Rare:24; Clinvar:1 | ||||
| chr9:35691067-35691255 | Common:1; Rare:40 | ||||
| chr9:35732083-35732326 | Common:2; Rare:67 | ||||
| chr9:35732373-35732751 | Common:3; Rare:97 | ||||
| chr9:35748993-35749395 | Common:2; Rare:150 | ||||
| chr9:35814983-35815281 | Rare:76 | ||||
| chr9:35829072-35829283 | Common:1; Rare:54 | ||||
| chr9:36036800-36036980 | Common:2; Rare:62 | ||||
| chr9:36190699-36191063 | Common:2; Rare:117 |