| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:57046464-57046758 | Rare:101 | ||||
| chr6:57046911-57046947 | Rare:2 | ||||
| chr6:57089692-57090227 | Common:2; Rare:175 | ||||
| chr6:57172374-57172933 | Common:2; Rare:168 | ||||
| chr6:57222266-57222353 | Rare:30 | ||||
| chr6:57317515-57317651 | Rare:36 | ||||
| chr6:62286093-62286352 | Common:1; Rare:79 | ||||
| chr6:63571930-63572030 | Rare:20 | ||||
| chr6:63572335-63572607 | Rare:103 | ||||
| chr6:63573331-63573530 | Rare:45 | ||||
| chr6:63635722-63636143 | Common:1; Rare:137 | ||||
| chr6:63636456-63636582 | Common:1; Rare:32 | ||||
| chr6:68634970-68635361 | Common:2; Rare:108 | ||||
| chr6:69796829-69797146 | Common:2; Rare:101; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:70413147-70413603 | Common:2; Rare:143 |