| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43770083-43770230 | Common:2; Rare:44 | ||||
| chr6:44127278-44127629 | Common:4; Rare:95 | ||||
| chr6:44219490-44219651 | Common:1; Rare:40 | ||||
| chr6:44387458-44387747 | Common:4; Rare:76 | ||||
| chr6:45377810-45378143 | Common:2; Rare:108 | ||||
| chr6:46129777-46130103 | Common:5; Rare:104 | ||||
| chr6:46652843-46653022 | Rare:41 | ||||
| chr6:47478067-47478242 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:49463167-49463401 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52420108-52420364 | Common:3; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52995275-52995844 | Common:4; Rare:235 | ||||
| chr6:53348864-53349211 | Common:2; Rare:139 | ||||
| chr6:53665696-53665879 | Common:1; Rare:42 | ||||
| chr6:56542770-56543014 | Common:2; Rare:43 | ||||
| chr6:63636068-63636143 | Rare:22 |