| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43575962-43576205 | Common:1; Rare:93; Clinvar:5 | ||||
| chr6:43635755-43635873 | Common:1; Rare:28 | ||||
| chr6:43687768-43687855 | Common:1; Rare:37 | ||||
| chr6:43771906-43771980 | Rare:16 | ||||
| chr6:44000301-44000622 | Common:1; Rare:70 | ||||
| chr6:44127361-44127631 | Common:4; Rare:76 | ||||
| chr6:44387445-44387747 | Common:4; Rare:79 | ||||
| chr6:46637260-46637467 | Rare:43 | ||||
| chr6:46652707-46653017 | Rare:78 | ||||
| chr6:49463178-49463412 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52284713-52284838 | Common:1; Rare:54 | ||||
| chr6:52420122-52420314 | Common:3; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52671041-52671167 | Rare:38 | ||||
| chr6:52995290-52995817 | Common:4; Rare:221 | ||||
| chr6:53348914-53349095 | Common:2; Rare:67 |