| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:121299624-121300004 | Common:3; Rare:118; Clinvar:3 | ||||
| chr9:121326415-121326751 | Common:5; Rare:113; Clinvar:3; Clinvar (benign):5 | ||||
| chr9:121328886-121329315 | Common:1; Rare:117; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:121370093-121370512 | Common:2; Rare:126 | ||||
| chr9:121566918-121567133 | Rare:54 | ||||
| chr9:122159689-122159933 | Rare:100 | ||||
| chr9:122264414-122264691 | Common:2; Rare:54 | ||||
| chr9:122264723-122264927 | Common:2; Rare:57 | ||||
| chr9:122905194-122905539 | Common:2; Rare:125 | ||||
| chr9:122913292-122913361 | Common:1; Rare:13 | ||||
| chr9:122931482-122931689 | Common:3; Rare:41 | ||||
| chr9:124940969-124941139 | Common:3; Rare:60 | ||||
| chr9:125189682-125190050 | Common:1; Rare:158 | ||||
| chr9:125200428-125200590 | Common:1; Rare:60 | ||||
| chr9:125241317-125241686 | Common:3; Rare:110 |