| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:110125345-110125546 | Rare:41 | ||||
| chr9:110256431-110256718 | Common:4; Rare:104 | ||||
| chr9:111038695-111038898 | Common:4; Rare:54 | ||||
| chr9:112379841-112380146 | Common:3; Rare:126 | ||||
| chr9:113056657-113056899 | Common:1; Rare:80; Clinvar:1 | ||||
| chr9:113221262-113221628 | Rare:114 | ||||
| chr9:113275371-113275726 | Common:5; Rare:111; Clinvar (pathogenic):1 | ||||
| chr9:113410289-113410569 | Common:1; Rare:93 | ||||
| chr9:113410662-113410683 | Rare:4 | ||||
| chr9:116687167-116687359 | Common:4; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120793263-120793533 | Common:1; Rare:99 | ||||
| chr9:120842917-120843121 | Common:1; Rare:70 | ||||
| chr9:121074848-121074969 | Rare:59 | ||||
| chr9:121201838-121202141 | Common:2; Rare:87 | ||||
| chr9:121268025-121268207 | Common:1; Rare:64 |