| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99221964-99222333 | Common:2; Rare:133 | ||||
| chr9:99906603-99906687 | Rare:41 | ||||
| chr9:100098972-100099314 | Common:3; Rare:94; Clinvar:2 | ||||
| chr9:100352903-100353082 | Rare:58 | ||||
| chr9:101398594-101398910 | Common:1; Rare:99 | ||||
| chr9:101533755-101533894 | Rare:38 | ||||
| chr9:112379848-112380138 | Common:2; Rare:121 | ||||
| chr9:113221294-113221584 | Rare:89 | ||||
| chr9:113275359-113275708 | Common:5; Rare:105; Clinvar (pathogenic):1 | ||||
| chr9:120842890-120843173 | Common:1; Rare:102 | ||||
| chr9:121201857-121202168 | Common:2; Rare:84 | ||||
| chr9:121268064-121268198 | Common:1; Rare:47 | ||||
| chr9:122264792-122264909 | Common:2; Rare:36 | ||||
| chr9:124861898-124862125 | Rare:96 | ||||
| chr9:125200421-125200557 | Common:1; Rare:45 |