| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:108934029-108934487 | Common:7; Rare:181; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109498246-109498464 | Rare:69 | ||||
| chr9:110125358-110125566 | Rare:44 | ||||
| chr9:110256410-110256671 | Common:2; Rare:95 | ||||
| chr9:110668752-110668814 | Rare:11 | ||||
| chr9:111599624-111599768 | Common:1; Rare:35 | ||||
| chr9:112379811-112380146 | Common:3; Rare:137 | ||||
| chr9:113056654-113056883 | Common:1; Rare:77; Clinvar:1 | ||||
| chr9:113221230-113221589 | Common:1; Rare:117 | ||||
| chr9:113275373-113275746 | Common:5; Rare:120; Clinvar (pathogenic):1 | ||||
| chr9:113410289-113410705 | Common:3; Rare:123 | ||||
| chr9:113463581-113463755 | Common:1; Rare:58 | ||||
| chr9:114387967-114388166 | Common:1; Rare:57 | ||||
| chr9:115118055-115118459 | Common:2; Rare:100 | ||||
| chr9:116687207-116687361 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):1 |