| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:107282991-107283289 | Common:1; Rare:101 | ||||
| chr9:107488439-107488582 | Common:1; Rare:43 | ||||
| chr9:107490117-107490335 | Rare:69 | ||||
| chr9:108934029-108934528 | Common:8; Rare:196; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109013420-109013760 | Common:2; Rare:117 | ||||
| chr9:109498236-109498479 | Rare:75 | ||||
| chr9:110125340-110125544 | Rare:42 | ||||
| chr9:110207525-110207654 | Rare:48 | ||||
| chr9:110256416-110256725 | Common:5; Rare:109 | ||||
| chr9:110580070-110580093 | Rare:3 | ||||
| chr9:111038699-111038915 | Common:4; Rare:57 | ||||
| chr9:111484212-111484360 | Rare:67 | ||||
| chr9:111599367-111599457 | Common:2; Rare:20 | ||||
| chr9:111661481-111661673 | Common:3; Rare:56 | ||||
| chr9:111896649-111896804 | Common:3; Rare:60 |