| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:93452294-93452372 | Rare:12 | ||||
| chr9:93453534-93453740 | Common:1; Rare:49 | ||||
| chr9:95003644-95004009 | Common:3; Rare:76 | ||||
| chr9:95004112-95004251 | Rare:42 | ||||
| chr9:95875453-95875737 | Common:1; Rare:100 | ||||
| chr9:95875961-95876037 | Common:4; Rare:37 | ||||
| chr9:96778054-96778156 | Rare:33 | ||||
| chr9:97633271-97633458 | Common:1; Rare:50 | ||||
| chr9:97633478-97633864 | Common:5; Rare:129 | ||||
| chr9:97697202-97697489 | Common:2; Rare:153; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr9:97922471-97922579 | Common:3; Rare:54 | ||||
| chr9:98255359-98255449 | Common:1; Rare:33 | ||||
| chr9:98255587-98255808 | Common:3; Rare:65 | ||||
| chr9:98943283-98943585 | Rare:53 | ||||
| chr9:98943604-98943951 | Common:5; Rare:106 |