| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:96418383-96418601 | Common:1; Rare:52 | ||||
| chr9:96449894-96450204 | Common:2; Rare:112 | ||||
| chr9:96619780-96620130 | Common:1; Rare:98 | ||||
| chr9:96655301-96655436 | Rare:34 | ||||
| chr9:96778057-96778290 | Common:2; Rare:65 | ||||
| chr9:96854315-96854649 | Common:4; Rare:84 | ||||
| chr9:96875894-96876102 | Rare:50 | ||||
| chr9:97013571-97013891 | Common:4; Rare:91 | ||||
| chr9:97039108-97039421 | Common:1; Rare:126 | ||||
| chr9:97633084-97633210 | Rare:52 | ||||
| chr9:97633256-97633481 | Common:1; Rare:60 | ||||
| chr9:97633657-97633830 | Common:2; Rare:55 | ||||
| chr9:97697264-97697497 | Common:2; Rare:125; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr9:97922149-97922321 | Common:1; Rare:65 | ||||
| chr9:97922484-97922633 | Common:3; Rare:69 |