| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44219496-44219645 | Rare:36 | ||||
| chr6:44246875-44247193 | Common:4; Rare:134 | ||||
| chr6:44257480-44257743 | Rare:72 | ||||
| chr6:44387407-44387738 | Common:4; Rare:80 | ||||
| chr6:45377866-45378198 | Common:2; Rare:116 | ||||
| chr6:47478067-47478260 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:49463167-49463434 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52420101-52420364 | Common:3; Rare:111; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52670992-52671154 | Rare:49 | ||||
| chr6:52995267-52995817 | Common:4; Rare:228 | ||||
| chr6:53061682-53062053 | Rare:84 | ||||
| chr6:53065379-53065603 | Common:1; Rare:68 | ||||
| chr6:53348853-53349227 | Common:2; Rare:153 | ||||
| chr6:56542792-56542980 | Common:1; Rare:31 | ||||
| chr6:56693276-56693508 | Rare:42 |