| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:77177465-77177714 | Common:2; Rare:75; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:78235977-78236155 | Rare:64 | ||||
| chr9:78296908-78297199 | Common:1; Rare:81 | ||||
| chr9:81689476-81689829 | Common:10; Rare:144 | ||||
| chr9:83267166-83267319 | Rare:34 | ||||
| chr9:83538315-83538488 | Common:1; Rare:59 | ||||
| chr9:83623052-83623155 | Common:1; Rare:24 | ||||
| chr9:83707073-83707288 | Common:1; Rare:70 | ||||
| chr9:83707671-83708343 | Common:6; Rare:229 | ||||
| chr9:83921414-83921599 | Common:2; Rare:75 | ||||
| chr9:83971670-83972188 | Rare:140; Clinvar:2 | ||||
| chr9:83979579-83979748 | Rare:57 | ||||
| chr9:83980146-83980382 | Common:1; Rare:89 | ||||
| chr9:83980501-83980860 | Common:5; Rare:147 | ||||
| chr9:85741849-85742264 | Common:5; Rare:157 |