| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34612090-34612265 | Common:8; Rare:62 | ||||
| chr9:34665381-34665665 | Rare:91 | ||||
| chr9:34666021-34666177 | Common:1; Rare:34 | ||||
| chr9:35657846-35657919 | Common:2; Rare:73; Clinvar:14; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr9:35657925-35658352 | Common:6; Rare:346; Clinvar:26; Clinvar (benign):13; Clinvar (pathogenic):36 | ||||
| chr9:35689702-35690123 | Common:4; Rare:130; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35732083-35732320 | Common:1; Rare:66 | ||||
| chr9:35732365-35732671 | Common:2; Rare:77 | ||||
| chr9:35748989-35749331 | Common:2; Rare:122 | ||||
| chr9:36258404-36258622 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37592539-37592643 | Common:2; Rare:37 | ||||
| chr9:37800707-37800794 | Rare:25 | ||||
| chr9:68356387-68356619 | Common:7; Rare:40 | ||||
| chr9:70258810-70259069 | Common:4; Rare:123 | ||||
| chr9:71911184-71911489 | Common:2; Rare:85 |