| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43575793-43576185 | Common:1; Rare:148; Clinvar:4 | ||||
| chr6:43625523-43625815 | Common:1; Rare:78 | ||||
| chr6:43629133-43629440 | Common:2; Rare:91 | ||||
| chr6:43635779-43635893 | Common:1; Rare:31 | ||||
| chr6:43644975-43645122 | Common:1; Rare:44; Clinvar (benign):1 | ||||
| chr6:43687750-43687846 | Common:1; Rare:42 | ||||
| chr6:43770070-43770221 | Common:2; Rare:45 | ||||
| chr6:43771906-43772006 | Rare:19 | ||||
| chr6:44126711-44127000 | Common:1; Rare:72 | ||||
| chr6:44127361-44127689 | Common:4; Rare:96 | ||||
| chr6:44138398-44138511 | Rare:26 | ||||
| chr6:44138642-44138831 | Common:8; Rare:52 | ||||
| chr6:44158759-44158849 | Rare:27 | ||||
| chr6:44219483-44219682 | Common:2; Rare:52 | ||||
| chr6:44226908-44227013 | Common:1; Rare:19 |