| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99221890-99222355 | Common:2; Rare:186; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:99906575-99906690 | Rare:60 | ||||
| chr9:100098974-100099307 | Common:2; Rare:91; Clinvar:1 | ||||
| chr9:100352860-100353085 | Rare:81 | ||||
| chr9:101398585-101398912 | Common:1; Rare:104 | ||||
| chr9:101533682-101533889 | Common:1; Rare:63 | ||||
| chr9:104093988-104094321 | Common:3; Rare:75 | ||||
| chr9:104094522-104094603 | Common:1; Rare:26 | ||||
| chr9:105557890-105558159 | Rare:68; Clinvar (benign):1 | ||||
| chr9:105694440-105694567 | Common:2; Rare:56 | ||||
| chr9:108934074-108934487 | Common:7; Rare:167; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109498246-109498433 | Rare:63 | ||||
| chr9:111661509-111661650 | Common:3; Rare:40 | ||||
| chr9:112379834-112380146 | Common:3; Rare:129 | ||||
| chr9:113056719-113056829 | Rare:33 |