| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128947598-128947718 | Common:1; Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129036359-129036672 | Common:2; Rare:86 | ||||
| chr9:129110602-129110949 | Common:3; Rare:78 | ||||
| chr9:129139901-129140148 | Rare:53 | ||||
| chr9:129178247-129178521 | Common:3; Rare:82 | ||||
| chr9:129642060-129642362 | Common:3; Rare:82 | ||||
| chr9:129753014-129753188 | Rare:45 | ||||
| chr9:129835210-129835498 | Common:3; Rare:115 | ||||
| chr9:130042956-130043307 | Common:2; Rare:102 | ||||
| chr9:130053854-130054025 | Common:1; Rare:66 | ||||
| chr9:130579456-130579692 | Common:6; Rare:98 | ||||
| chr9:130693502-130693805 | Rare:88 | ||||
| chr9:130835095-130835459 | Common:11; Rare:114 | ||||
| chr9:131125416-131125637 | Common:2; Rare:102 | ||||
| chr9:131502886-131503062 | Rare:63; Clinvar:3 |