| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:107459439-107459778 | Common:2; Rare:88; Clinvar:1 | ||||
| chr6:107490438-107490590 | Common:2; Rare:53 | ||||
| chr6:107958069-107958411 | Common:2; Rare:104; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:108074659-108074866 | Common:1; Rare:69; Clinvar:1 | ||||
| chr6:108260765-108260847 | Rare:23 | ||||
| chr6:108260907-108261356 | Common:2; Rare:184 | ||||
| chr6:108294786-108295097 | Common:1; Rare:85 | ||||
| chr6:108560729-108560917 | Rare:84 | ||||
| chr6:108848186-108848496 | Common:1; Rare:103 | ||||
| chr6:109009432-109009689 | Common:2; Rare:80 | ||||
| chr6:109094452-109094631 | Rare:46 | ||||
| chr6:109094820-109095163 | Common:3; Rare:99 | ||||
| chr6:109382058-109382286 | Common:4; Rare:89 | ||||
| chr6:109382297-109382324 | Rare:11 | ||||
| chr6:109382379-109382860 | Common:7; Rare:157; Clinvar (benign):1 |