| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:120929120-120929173 | Common:1; Rare:13 | ||||
| chr9:121074851-121074984 | Rare:68 | ||||
| chr9:121201824-121202158 | Common:2; Rare:101 | ||||
| chr9:121268068-121268207 | Common:1; Rare:45 | ||||
| chr9:121285833-121286107 | Common:2; Rare:45 | ||||
| chr9:121299656-121300004 | Common:3; Rare:114; Clinvar:3 | ||||
| chr9:121326381-121326767 | Common:5; Rare:124; Clinvar:3; Clinvar (benign):5 | ||||
| chr9:121328890-121329315 | Common:1; Rare:116; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:121370183-121370453 | Common:2; Rare:80 | ||||
| chr9:122264586-122264685 | Common:1; Rare:21 | ||||
| chr9:122264731-122264935 | Common:2; Rare:61 | ||||
| chr9:122370962-122371068 | Rare:34 | ||||
| chr9:122905186-122905417 | Common:1; Rare:100 | ||||
| chr9:122913277-122913431 | Common:3; Rare:36 | ||||
| chr9:122931464-122931717 | Common:3; Rare:56 |