| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:108934074-108934471 | Common:7; Rare:157; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:110125340-110125576 | Rare:47 | ||||
| chr9:110256414-110256684 | Common:2; Rare:97 | ||||
| chr9:110579178-110579323 | Rare:44 | ||||
| chr9:111599389-111599534 | Common:1; Rare:34 | ||||
| chr9:111599623-111599937 | Common:2; Rare:84 | ||||
| chr9:111661481-111661673 | Common:3; Rare:56 | ||||
| chr9:112379772-112380150 | Common:4; Rare:147 | ||||
| chr9:113056681-113056883 | Rare:69 | ||||
| chr9:113221262-113221640 | Rare:118 | ||||
| chr9:113275392-113275734 | Common:5; Rare:113; Clinvar (pathogenic):1 | ||||
| chr9:114587415-114587867 | Common:4; Rare:156 | ||||
| chr9:116153566-116153895 | Common:1; Rare:75 | ||||
| chr9:116687207-116687364 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120793263-120793526 | Common:1; Rare:94 |