| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:120714468-120714747 | Common:2; Rare:93 | ||||
| chr9:120793232-120793538 | Common:2; Rare:112 | ||||
| chr9:120842905-120843259 | Common:1; Rare:112 | ||||
| chr9:120868850-120869093 | Common:2; Rare:50 | ||||
| chr9:120929146-120929202 | Common:1; Rare:14 | ||||
| chr9:121074849-121074969 | Rare:59 | ||||
| chr9:121201811-121202158 | Common:2; Rare:107 | ||||
| chr9:121268050-121268198 | Common:1; Rare:52 | ||||
| chr9:121285851-121286107 | Common:1; Rare:43 | ||||
| chr9:121299722-121299831 | Rare:33; Clinvar:1 | ||||
| chr9:121329080-121329315 | Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:121370187-121370527 | Common:2; Rare:101 | ||||
| chr9:122159696-122159933 | Rare:94 | ||||
| chr9:122264333-122264691 | Common:3; Rare:73 | ||||
| chr9:122264742-122264922 | Common:2; Rare:51 |