| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:120714445-120714706 | Common:2; Rare:83 | ||||
| chr9:120793248-120793548 | Common:2; Rare:111 | ||||
| chr9:120842884-120843268 | Common:1; Rare:127 | ||||
| chr9:120877129-120877466 | Common:3; Rare:106 | ||||
| chr9:121050183-121050503 | Rare:78; Clinvar (pathogenic):1 | ||||
| chr9:121074827-121074992 | Rare:85 | ||||
| chr9:121201819-121202182 | Common:2; Rare:110 | ||||
| chr9:121326157-121326397 | Common:2; Rare:41 | ||||
| chr9:121329110-121329315 | Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:121370172-121370578 | Common:2; Rare:117 | ||||
| chr9:122159714-122159916 | Rare:73 | ||||
| chr9:122264577-122264690 | Common:2; Rare:28 | ||||
| chr9:122264748-122264925 | Common:2; Rare:51 | ||||
| chr9:122913277-122913377 | Common:2; Rare:23 | ||||
| chr9:122931482-122931694 | Common:3; Rare:44 |