| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:121201832-121202149 | Common:2; Rare:93 | ||||
| chr9:121268016-121268213 | Common:1; Rare:69 | ||||
| chr9:121326243-121326767 | Common:5; Rare:144; Clinvar:3; Clinvar (benign):5 | ||||
| chr9:121370183-121370379 | Common:1; Rare:50 | ||||
| chr9:122264768-122264922 | Common:2; Rare:46 | ||||
| chr9:124861908-124862125 | Rare:93 | ||||
| chr9:124940969-124941156 | Common:3; Rare:62 | ||||
| chr9:125200440-125200566 | Common:1; Rare:44 | ||||
| chr9:126860589-126860711 | Common:2; Rare:41 | ||||
| chr9:127224375-127224621 | Rare:69 | ||||
| chr9:127424253-127424478 | Common:1; Rare:74 | ||||
| chr9:127451257-127451584 | Common:3; Rare:131; Clinvar (benign):1 | ||||
| chr9:128191448-128191629 | Rare:56 | ||||
| chr9:128275909-128276293 | Common:4; Rare:167 | ||||
| chr9:128322410-128322627 | Common:1; Rare:61 |