| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:106863539-106863669 | Rare:23 | ||||
| chr9:107282951-107283317 | Common:3; Rare:129 | ||||
| chr9:107283403-107283681 | Common:3; Rare:68 | ||||
| chr9:107488730-107488821 | Rare:30 | ||||
| chr9:107489752-107490084 | Common:4; Rare:145 | ||||
| chr9:107490227-107490341 | Rare:35 | ||||
| chr9:108934055-108934471 | Common:7; Rare:162; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109013471-109013666 | Common:2; Rare:72 | ||||
| chr9:109497868-109497995 | Common:1; Rare:42 | ||||
| chr9:109498227-109498484 | Common:1; Rare:78 | ||||
| chr9:110125413-110125553 | Rare:29 | ||||
| chr9:110207512-110207654 | Rare:50 | ||||
| chr9:110256410-110256718 | Common:4; Rare:107 | ||||
| chr9:111038692-111038980 | Common:5; Rare:68 | ||||
| chr9:111631131-111631367 | Common:1; Rare:63 |