| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:104093987-104094312 | Common:3; Rare:75 | ||||
| chr9:108934082-108934471 | Common:7; Rare:154; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:112379834-112380142 | Common:3; Rare:129 | ||||
| chr9:113221267-113221617 | Rare:105 | ||||
| chr9:113275380-113275726 | Common:5; Rare:111; Clinvar (pathogenic):1 | ||||
| chr9:113410281-113410741 | Common:4; Rare:143 | ||||
| chr9:114587634-114587846 | Common:1; Rare:78 | ||||
| chr9:120793374-120793526 | Rare:54 | ||||
| chr9:120842884-120843242 | Common:1; Rare:122 | ||||
| chr9:120877109-120877451 | Common:2; Rare:97 | ||||
| chr9:121201830-121202168 | Common:2; Rare:98 | ||||
| chr9:121370194-121370516 | Common:2; Rare:98 | ||||
| chr9:122264770-122264915 | Common:2; Rare:43 | ||||
| chr9:122913316-122913426 | Common:2; Rare:28 | ||||
| chr9:122931490-122931680 | Common:3; Rare:36 |