| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:99549534-99549826 | Rare:47 | ||||
| chr6:100881068-100881506 | Common:7; Rare:142 | ||||
| chr6:106325551-106325916 | Common:1; Rare:126 | ||||
| chr6:106629443-106629677 | Common:4; Rare:56 | ||||
| chr6:106975302-106975396 | Rare:29 | ||||
| chr6:107028096-107028397 | Common:2; Rare:100 | ||||
| chr6:107459479-107459606 | Rare:36; Clinvar:1 | ||||
| chr6:107824076-107824185 | Rare:25 | ||||
| chr6:107958034-107958429 | Common:2; Rare:123; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:108074661-108074888 | Common:1; Rare:78; Clinvar:1 | ||||
| chr6:108260764-108261093 | Rare:135 | ||||
| chr6:108294782-108295077 | Common:1; Rare:80 | ||||
| chr6:108560730-108560917 | Rare:84 | ||||
| chr6:108848332-108848475 | Rare:52 | ||||
| chr6:109009476-109009689 | Common:2; Rare:68 |