| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35079926-35080170 | Common:4; Rare:65; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:35103073-35103297 | Common:1; Rare:83 | ||||
| chr9:35489916-35490139 | Common:2; Rare:64 | ||||
| chr9:35646805-35646971 | Common:1; Rare:40 | ||||
| chr9:35657868-35658386 | Common:7; Rare:427; Clinvar:38; Clinvar (benign):14; Clinvar (pathogenic):40 | ||||
| chr9:35685432-35685781 | Common:1; Rare:81; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr9:35689702-35690120 | Common:4; Rare:129; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35732073-35732334 | Common:2; Rare:70 | ||||
| chr9:35732364-35732683 | Common:3; Rare:81 | ||||
| chr9:35748999-35749369 | Common:2; Rare:139 | ||||
| chr9:35814983-35815302 | Rare:82 | ||||
| chr9:36190642-36190994 | Common:1; Rare:111 | ||||
| chr9:36258402-36258607 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37592471-37592791 | Common:2; Rare:97 | ||||
| chr9:37785024-37785132 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):2 |