| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:120793242-120793538 | Common:2; Rare:108 | ||||
| chr9:120842910-120843282 | Common:1; Rare:121 | ||||
| chr9:120868818-120869137 | Common:2; Rare:75 | ||||
| chr9:120877186-120877512 | Common:1; Rare:113 | ||||
| chr9:120929123-120929155 | Common:1; Rare:5 | ||||
| chr9:121074842-121075000 | Rare:83 | ||||
| chr9:121075109-121075317 | Rare:51 | ||||
| chr9:121201814-121202158 | Common:2; Rare:107 | ||||
| chr9:121268064-121268203 | Common:1; Rare:48 | ||||
| chr9:121286048-121286150 | Rare:27 | ||||
| chr9:121299577-121300012 | Common:5; Rare:138; Clinvar:3 | ||||
| chr9:121326228-121326769 | Common:5; Rare:148; Clinvar:3; Clinvar (benign):5 | ||||
| chr9:121328886-121329315 | Common:1; Rare:117; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:121370113-121370536 | Common:2; Rare:123 | ||||
| chr9:122159716-122159898 | Rare:67 |