| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:116687203-116687370 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:120793255-120793543 | Common:2; Rare:107 | ||||
| chr9:120842901-120843084 | Common:1; Rare:64 | ||||
| chr9:120877186-120877492 | Common:1; Rare:101 | ||||
| chr9:121074837-121074967 | Rare:60 | ||||
| chr9:121121668-121121831 | Rare:44 | ||||
| chr9:121201829-121202174 | Common:2; Rare:99 | ||||
| chr9:121268071-121268207 | Common:1; Rare:44 | ||||
| chr9:121370184-121370461 | Common:2; Rare:82 | ||||
| chr9:122159674-122159908 | Rare:101 | ||||
| chr9:122264737-122264922 | Common:2; Rare:53 | ||||
| chr9:122905281-122905591 | Common:2; Rare:113 | ||||
| chr9:122931488-122931719 | Common:3; Rare:50 | ||||
| chr9:122940779-122941050 | Common:2; Rare:106 | ||||
| chr9:124861903-124862134 | Common:1; Rare:96 |