| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:99424663-99424963 | Rare:82 | ||||
| chr6:99425214-99425506 | Common:2; Rare:86 | ||||
| chr6:99515401-99515479 | Rare:28 | ||||
| chr6:100464876-100465098 | Common:2; Rare:59 | ||||
| chr6:100881189-100881482 | Common:6; Rare:105 | ||||
| chr6:106325551-106325847 | Rare:97 | ||||
| chr6:106629448-106629645 | Common:3; Rare:46 | ||||
| chr6:107459490-107459756 | Common:2; Rare:68; Clinvar:1 | ||||
| chr6:107958097-107958416 | Common:1; Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:108074611-108074866 | Common:1; Rare:88; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr6:108260764-108260815 | Rare:14 | ||||
| chr6:108260862-108261302 | Common:2; Rare:172 | ||||
| chr6:108294802-108295071 | Common:1; Rare:72 | ||||
| chr6:108560729-108560975 | Rare:100 | ||||
| chr6:108848317-108848496 | Rare:66 |