| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:108934055-108934510 | Common:7; Rare:183; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109498278-109498419 | Rare:51 | ||||
| chr9:110125374-110125542 | Rare:35 | ||||
| chr9:110256431-110256718 | Common:4; Rare:104 | ||||
| chr9:111599617-111599894 | Common:2; Rare:78 | ||||
| chr9:111661366-111661659 | Common:3; Rare:71 | ||||
| chr9:112379834-112380140 | Common:3; Rare:125 | ||||
| chr9:112718072-112718152 | Rare:17 | ||||
| chr9:113056631-113056861 | Common:1; Rare:78; Clinvar:1 | ||||
| chr9:113150932-113151015 | Rare:26 | ||||
| chr9:113221262-113221617 | Rare:110 | ||||
| chr9:113275392-113275734 | Common:5; Rare:113; Clinvar (pathogenic):1 | ||||
| chr9:113340290-113340402 | Common:1; Rare:23 | ||||
| chr9:113410289-113410705 | Common:3; Rare:123 | ||||
| chr9:114587565-114587865 | Common:3; Rare:120 |