| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:52420108-52420376 | Common:3; Rare:114; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52576944-52577294 | Common:6; Rare:120 | ||||
| chr6:52671053-52671190 | Rare:38 | ||||
| chr6:52995249-52995808 | Common:4; Rare:231 | ||||
| chr6:53348853-53349054 | Common:1; Rare:104 | ||||
| chr6:53349146-53349167 | Rare:6 | ||||
| chr6:56542736-56543065 | Common:2; Rare:56 | ||||
| chr6:57089822-57090200 | Rare:127 | ||||
| chr6:57172556-57172798 | Common:1; Rare:78 | ||||
| chr6:57221404-57221558 | Rare:37 | ||||
| chr6:57222021-57222391 | Rare:133 | ||||
| chr6:57317515-57317684 | Rare:48 | ||||
| chr6:63572297-63572622 | Rare:122 | ||||
| chr6:69796862-69797151 | Common:1; Rare:88; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:70667664-70667960 | Common:3; Rare:104 |