| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33025077-33025301 | Common:6; Rare:91 | ||||
| chr9:33166837-33166907 | Rare:22; Clinvar:1 | ||||
| chr9:33290255-33290571 | Common:3; Rare:108 | ||||
| chr9:34329303-34329592 | Rare:77 | ||||
| chr9:34652050-34652214 | Rare:48 | ||||
| chr9:35489922-35490108 | Common:1; Rare:51 | ||||
| chr9:35657857-35657923 | Common:2; Rare:67; Clinvar:14; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr9:35657925-35658371 | Common:6; Rare:356; Clinvar:26; Clinvar (benign):13; Clinvar (pathogenic):36 | ||||
| chr9:35689702-35690120 | Common:4; Rare:129; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35732073-35732310 | Common:1; Rare:63 | ||||
| chr9:35732373-35732676 | Common:2; Rare:76 | ||||
| chr9:35748998-35749347 | Common:2; Rare:132 | ||||
| chr9:35814984-35815293 | Rare:79 | ||||
| chr9:36036800-36036980 | Common:2; Rare:62 | ||||
| chr9:36258409-36258607 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):1 |