| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43771664-43772000 | Common:4; Rare:59 | ||||
| chr6:43774058-43774392 | Rare:79 | ||||
| chr6:44127278-44127675 | Common:4; Rare:111 | ||||
| chr6:44219474-44219699 | Common:2; Rare:66 | ||||
| chr6:44246880-44247193 | Common:4; Rare:132 | ||||
| chr6:44257342-44257633 | Rare:86 | ||||
| chr6:44387441-44387770 | Common:4; Rare:88 | ||||
| chr6:45377782-45378173 | Common:2; Rare:124 | ||||
| chr6:46015490-46015555 | Rare:20 | ||||
| chr6:46129777-46129993 | Common:3; Rare:56 | ||||
| chr6:46652789-46653013 | Rare:56 | ||||
| chr6:47477570-47478023 | Common:2; Rare:123; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:47478068-47478280 | Common:2; Rare:79; Clinvar:2; Clinvar (benign):4 | ||||
| chr6:48068826-48068951 | Common:1; Rare:37 | ||||
| chr6:49463122-49463417 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):1 |