| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:108933917-108934510 | Common:9; Rare:235; Clinvar:7; Clinvar (benign):3 | ||||
| chr9:109013445-109013773 | Common:2; Rare:116 | ||||
| chr9:109013897-109013996 | Common:2; Rare:24 | ||||
| chr9:110256426-110256729 | Common:5; Rare:107 | ||||
| chr9:110579704-110579838 | Common:1; Rare:33 | ||||
| chr9:111631180-111631386 | Common:1; Rare:57 | ||||
| chr9:112379811-112380153 | Common:3; Rare:138 | ||||
| chr9:113056674-113056861 | Rare:65 | ||||
| chr9:113221227-113221659 | Common:1; Rare:133 | ||||
| chr9:113275382-113275735 | Common:5; Rare:115; Clinvar (pathogenic):1 | ||||
| chr9:113410308-113410582 | Common:1; Rare:87 | ||||
| chr9:114387978-114388104 | Common:1; Rare:44 | ||||
| chr9:114587702-114587845 | Common:1; Rare:62 | ||||
| chr9:115118008-115118354 | Common:3; Rare:85 | ||||
| chr9:116153565-116153866 | Common:1; Rare:70 |