| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113056657-113056935 | Common:1; Rare:87; Clinvar:1 | ||||
| chr9:113188006-113188176 | Common:2; Rare:21 | ||||
| chr9:113221230-113221620 | Common:1; Rare:123 | ||||
| chr9:113275354-113275746 | Common:5; Rare:128; Clinvar (pathogenic):1 | ||||
| chr9:113410201-113410736 | Common:3; Rare:169 | ||||
| chr9:113593848-113594184 | Common:6; Rare:126 | ||||
| chr9:116687207-116687361 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120580123-120580241 | Rare:37; Clinvar:5 | ||||
| chr9:120793248-120793538 | Common:2; Rare:107 | ||||
| chr9:120842891-120843239 | Common:1; Rare:118 | ||||
| chr9:120877118-120877507 | Common:3; Rare:127 | ||||
| chr9:121074849-121074969 | Rare:59 | ||||
| chr9:121201832-121202161 | Common:2; Rare:96 | ||||
| chr9:121285849-121286111 | Common:1; Rare:43 | ||||
| chr9:121326088-121326416 | Common:2; Rare:51 |