| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:52420089-52420364 | Common:3; Rare:117; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52995307-52995714 | Common:4; Rare:163 | ||||
| chr6:53065379-53065618 | Common:1; Rare:72 | ||||
| chr6:53348882-53349020 | Common:1; Rare:74 | ||||
| chr6:53349156-53349187 | Rare:6 | ||||
| chr6:57046455-57046747 | Rare:106 | ||||
| chr6:57089906-57090200 | Rare:103 | ||||
| chr6:57317526-57317674 | Rare:41 | ||||
| chr6:69796899-69797126 | Rare:64; Clinvar:4 | ||||
| chr6:70566856-70566952 | Common:1; Rare:36 | ||||
| chr6:73521597-73521695 | Rare:23 | ||||
| chr6:73696034-73696236 | Rare:49 | ||||
| chr6:75284728-75285033 | Common:1; Rare:88 | ||||
| chr6:79537367-79537566 | Common:2; Rare:53; Clinvar:4 | ||||
| chr6:80004484-80004692 | Common:4; Rare:52 |