| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43575962-43576185 | Rare:87; Clinvar:4 | ||||
| chr6:43635760-43635893 | Common:1; Rare:36 | ||||
| chr6:43687750-43687825 | Common:1; Rare:30 | ||||
| chr6:43770088-43770230 | Common:2; Rare:43 | ||||
| chr6:43771927-43772008 | Rare:12 | ||||
| chr6:44127346-44127657 | Common:4; Rare:92 | ||||
| chr6:44223478-44223790 | Common:2; Rare:95 | ||||
| chr6:44229589-44229930 | Rare:92 | ||||
| chr6:46015490-46015564 | Rare:22 | ||||
| chr6:46129777-46130082 | Common:5; Rare:95 | ||||
| chr6:46491172-46491603 | Common:2; Rare:122 | ||||
| chr6:46491934-46492071 | Rare:21 | ||||
| chr6:46652707-46653013 | Rare:77 | ||||
| chr6:46921827-46922080 | Common:3; Rare:67 | ||||
| chr6:49463161-49463391 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 |