| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:107490432-107490618 | Common:3; Rare:67 | ||||
| chr6:107958005-107958418 | Common:2; Rare:133; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:108074600-108074866 | Common:1; Rare:92; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr6:108260764-108261325 | Common:2; Rare:214 | ||||
| chr6:108294791-108295158 | Common:2; Rare:122 | ||||
| chr6:108560726-108560960 | Rare:98 | ||||
| chr6:108848354-108848503 | Rare:55 | ||||
| chr6:108848635-108848797 | Rare:38 | ||||
| chr6:109009405-109009689 | Common:2; Rare:84 | ||||
| chr6:109093953-109094499 | Rare:137 | ||||
| chr6:109094503-109094539 | Rare:6 | ||||
| chr6:109094820-109095221 | Common:5; Rare:122 | ||||
| chr6:109095415-109095551 | Rare:29 | ||||
| chr6:109382210-109382896 | Common:8; Rare:242; Clinvar (benign):2 | ||||
| chr6:109440343-109440388 | Rare:17 |