| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:100881075-100881482 | Common:7; Rare:132 | ||||
| chr6:106325411-106325485 | Common:1; Rare:14 | ||||
| chr6:106325571-106325906 | Common:1; Rare:114 | ||||
| chr6:106629448-106629661 | Common:3; Rare:51 | ||||
| chr6:106975270-106975536 | Common:1; Rare:76 | ||||
| chr6:107459490-107459702 | Common:1; Rare:52; Clinvar:1 | ||||
| chr6:107958088-107958416 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:108074615-108074866 | Common:1; Rare:85; Clinvar:1 | ||||
| chr6:108260830-108261012 | Rare:89 | ||||
| chr6:108294769-108295076 | Common:1; Rare:82 | ||||
| chr6:109095407-109095561 | Rare:33 | ||||
| chr6:109382214-109382286 | Rare:30 | ||||
| chr6:109382302-109382328 | Rare:11 | ||||
| chr6:109382332-109382838 | Common:6; Rare:168; Clinvar (benign):2 | ||||
| chr6:109440575-109440868 | Common:2; Rare:102 |