| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:110580004-110580160 | Rare:27 | ||||
| chr9:111038673-111038868 | Common:4; Rare:52 | ||||
| chr9:111661455-111661673 | Common:3; Rare:63 | ||||
| chr9:112379770-112380146 | Common:4; Rare:146 | ||||
| chr9:113056651-113056909 | Common:1; Rare:82; Clinvar:1 | ||||
| chr9:113188033-113188176 | Common:2; Rare:16 | ||||
| chr9:113221229-113221607 | Common:1; Rare:121 | ||||
| chr9:113275359-113275734 | Common:5; Rare:119; Clinvar (pathogenic):1 | ||||
| chr9:113410298-113410748 | Common:4; Rare:139 | ||||
| chr9:113565097-113565181 | Common:1; Rare:17 | ||||
| chr9:114387949-114388176 | Common:1; Rare:62 | ||||
| chr9:115118134-115118433 | Rare:71 | ||||
| chr9:116687207-116687361 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120580125-120580360 | Common:1; Rare:77; Clinvar:5 | ||||
| chr9:120793244-120793526 | Common:1; Rare:99 |