| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:106862975-106863120 | Rare:57 | ||||
| chr9:108934108-108934486 | Common:6; Rare:156; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:110256450-110256720 | Common:4; Rare:99 | ||||
| chr9:111631137-111631386 | Common:1; Rare:69 | ||||
| chr9:111661509-111661667 | Common:3; Rare:49 | ||||
| chr9:111897217-111897264 | Rare:20 | ||||
| chr9:112379871-112380139 | Common:1; Rare:113 | ||||
| chr9:113221222-113221621 | Common:1; Rare:128 | ||||
| chr9:113275392-113275708 | Common:5; Rare:99; Clinvar (pathogenic):1 | ||||
| chr9:114505441-114505705 | Common:2; Rare:76 | ||||
| chr9:116687235-116687376 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:120793374-120793543 | Common:1; Rare:64 | ||||
| chr9:121201857-121202202 | Common:2; Rare:94 | ||||
| chr9:121370192-121370520 | Common:2; Rare:99 | ||||
| chr9:122264748-122264915 | Common:2; Rare:48 |