| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:112379848-112380146 | Common:2; Rare:126 | ||||
| chr9:112718086-112718417 | Rare:72 | ||||
| chr9:113221230-113221619 | Common:1; Rare:122 | ||||
| chr9:113275381-113275720 | Common:5; Rare:107; Clinvar (pathogenic):1 | ||||
| chr9:113340290-113340402 | Common:1; Rare:23 | ||||
| chr9:113401248-113401545 | Common:6; Rare:111; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410281-113410790 | Common:4; Rare:164 | ||||
| chr9:114388054-114388132 | Rare:22 | ||||
| chr9:114587628-114587910 | Common:1; Rare:100 | ||||
| chr9:116687228-116687361 | Common:1; Rare:43; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120580135-120580381 | Common:1; Rare:77; Clinvar:3 | ||||
| chr9:120793248-120793543 | Common:2; Rare:109 | ||||
| chr9:120842890-120843121 | Common:1; Rare:87 | ||||
| chr9:120877163-120877554 | Common:2; Rare:134 | ||||
| chr9:121074513-121074565 | Rare:19 |