| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:53348892-53349227 | Common:2; Rare:123 | ||||
| chr6:53545098-53545239 | Rare:40 | ||||
| chr6:56542882-56543017 | Common:1; Rare:19 | ||||
| chr6:56842710-56842820 | Rare:21 | ||||
| chr6:57046464-57046758 | Rare:101 | ||||
| chr6:57172369-57172712 | Common:1; Rare:100 | ||||
| chr6:57222266-57222380 | Rare:45 | ||||
| chr6:57317539-57317658 | Rare:35 | ||||
| chr6:63571512-63571830 | Common:1; Rare:75 | ||||
| chr6:63572218-63572753 | Rare:174 | ||||
| chr6:63573453-63573815 | Rare:95 | ||||
| chr6:63636045-63636149 | Rare:34 | ||||
| chr6:68634926-68635520 | Common:3; Rare:152 | ||||
| chr6:69796847-69797174 | Common:1; Rare:102; Clinvar:6; Clinvar (benign):3 | ||||
| chr6:69866007-69866131 | Common:1; Rare:9 |