| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:110125384-110125553 | Rare:35 | ||||
| chr9:110207519-110207685 | Rare:60 | ||||
| chr9:111038199-111038387 | Common:2; Rare:58 | ||||
| chr9:112379759-112380150 | Common:4; Rare:151 | ||||
| chr9:113221262-113221597 | Rare:106 | ||||
| chr9:113275354-113275728 | Common:5; Rare:121; Clinvar (pathogenic):1 | ||||
| chr9:113410289-113410724 | Common:3; Rare:130 | ||||
| chr9:116687235-116687364 | Common:1; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120793248-120793534 | Common:1; Rare:104 | ||||
| chr9:120842909-120843121 | Common:1; Rare:78 | ||||
| chr9:121074849-121074981 | Rare:66 | ||||
| chr9:121075109-121075185 | Rare:24 | ||||
| chr9:121201838-121202158 | Common:2; Rare:91 | ||||
| chr9:121370192-121370453 | Common:2; Rare:77 | ||||
| chr9:122159723-122159953 | Rare:81 |