| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:106862968-106863162 | Rare:66 | ||||
| chr9:108934015-108934484 | Common:7; Rare:184; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:110579084-110579299 | Rare:54 | ||||
| chr9:111631137-111631386 | Common:1; Rare:69 | ||||
| chr9:112379800-112380148 | Common:3; Rare:140 | ||||
| chr9:113221247-113221603 | Common:1; Rare:114 | ||||
| chr9:113275397-113275720 | Common:5; Rare:105; Clinvar (pathogenic):1 | ||||
| chr9:116153565-116153866 | Common:1; Rare:70 | ||||
| chr9:116687228-116687384 | Common:1; Rare:49; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:120793366-120793528 | Rare:62 | ||||
| chr9:120842779-120843084 | Common:3; Rare:118 | ||||
| chr9:121201852-121202139 | Common:2; Rare:80 | ||||
| chr9:121370208-121370520 | Common:2; Rare:92 | ||||
| chr9:122264778-122264919 | Common:2; Rare:43 | ||||
| chr9:122913242-122913434 | Common:3; Rare:42 |