| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113580674-113580927 | Common:3; Rare:47 | ||||
| chr9:116687228-116687334 | Common:1; Rare:27; Clinvar (benign):1 | ||||
| chr9:120793381-120793522 | Rare:47 | ||||
| chr9:120842916-120843193 | Common:1; Rare:89 | ||||
| chr9:120877148-120877512 | Common:3; Rare:125 | ||||
| chr9:121074709-121074981 | Rare:117 | ||||
| chr9:121201837-121202179 | Common:2; Rare:96 | ||||
| chr9:121268068-121268219 | Common:1; Rare:49 | ||||
| chr9:122264774-122264925 | Common:2; Rare:45 | ||||
| chr9:122913305-122913431 | Common:2; Rare:30 | ||||
| chr9:122931493-122931717 | Common:3; Rare:49 | ||||
| chr9:124861908-124862145 | Common:1; Rare:103 | ||||
| chr9:125200448-125200590 | Rare:54 | ||||
| chr9:127451311-127451520 | Common:2; Rare:93 | ||||
| chr9:128149285-128149520 | Rare:50 |