| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125238680-125239512 | Common:2; Rare:348 | ||||
| chr9:125746078-125746313 | Common:1; Rare:91 | ||||
| chr9:125746491-125746813 | Common:3; Rare:209 | ||||
| chr9:127049185-127049324 | Rare:14 | ||||
| chr9:127531497-127532001 | Common:1; Rare:204 | ||||
| chr9:127561660-127562310 | Common:5; Rare:129 | ||||
| chr9:127608394-127608901 | Common:3; Rare:159 | ||||
| chr9:127653670-127654000 | Common:1; Rare:74; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr9:127723490-127723800 | Common:1; Rare:64 | ||||
| chr9:127965450-127965860 | Common:12; Rare:139 | ||||
| chr9:128001611-128002250 | Common:2; Rare:139 | ||||
| chr9:128193010-128193680 | Common:4; Rare:164 | ||||
| chr9:128703237-128703605 | Common:1; Rare:95 | ||||
| chr9:129140735-129140882 | Common:4; Rare:65 | ||||
| chr9:129167135-129167287 | Common:2; Rare:39 |