| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111599608-111599902 | Common:2; Rare:83 | ||||
| chr9:112379765-112380146 | Common:4; Rare:146 | ||||
| chr9:113056674-113056911 | Rare:78 | ||||
| chr9:113221257-113221628 | Common:1; Rare:116 | ||||
| chr9:113275392-113275726 | Common:5; Rare:110; Clinvar (pathogenic):1 | ||||
| chr9:113410428-113410756 | Common:3; Rare:91 | ||||
| chr9:116687225-116687352 | Common:3; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:120580132-120580393 | Common:1; Rare:80; Clinvar:3 | ||||
| chr9:120793343-120793522 | Common:1; Rare:72 | ||||
| chr9:120842916-120843089 | Common:1; Rare:58 | ||||
| chr9:121201852-121202149 | Common:2; Rare:83 | ||||
| chr9:121370231-121370458 | Common:1; Rare:57 | ||||
| chr9:122159702-122159885 | Rare:75 | ||||
| chr9:122264778-122264923 | Common:2; Rare:44 | ||||
| chr9:124861879-124862151 | Common:1; Rare:122 |