| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111661514-111661698 | Common:3; Rare:55 | ||||
| chr9:112379759-112380154 | Common:4; Rare:151 | ||||
| chr9:112718002-112718370 | Common:2; Rare:87 | ||||
| chr9:113056615-113056924 | Common:1; Rare:101; Clinvar:1 | ||||
| chr9:113150890-113151017 | Rare:36 | ||||
| chr9:113221223-113221620 | Common:1; Rare:127 | ||||
| chr9:113275129-113275763 | Common:5; Rare:198; Clinvar (pathogenic):1 | ||||
| chr9:113340223-113340328 | Common:2; Rare:30 | ||||
| chr9:113401241-113401556 | Common:6; Rare:117; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410281-113410724 | Common:3; Rare:132 | ||||
| chr9:113565390-113565690 | Common:1; Rare:69 | ||||
| chr9:113593890-113594160 | Common:4; Rare:108 | ||||
| chr9:114587554-114587923 | Common:3; Rare:147 | ||||
| chr9:115118003-115118167 | Common:3; Rare:39 | ||||
| chr9:116687235-116687370 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):2 |