| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42929226-42929562 | Common:3; Rare:94 | ||||
| chr6:42984327-42984619 | Rare:71 | ||||
| chr6:43013822-43014276 | Common:2; Rare:114 | ||||
| chr6:43427783-43427880 | Rare:19 | ||||
| chr6:43516782-43517141 | Common:6; Rare:131; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575962-43576211 | Common:1; Rare:98; Clinvar:6 | ||||
| chr6:43687765-43687841 | Common:1; Rare:32 | ||||
| chr6:43770088-43770215 | Common:2; Rare:40 | ||||
| chr6:44127351-44127639 | Common:4; Rare:81 | ||||
| chr6:44246902-44247204 | Common:4; Rare:129 | ||||
| chr6:44387407-44387574 | Common:2; Rare:33 | ||||
| chr6:44387658-44387747 | Common:2; Rare:32 | ||||
| chr6:45377866-45378176 | Common:2; Rare:110 | ||||
| chr6:46921870-46921990 | Common:2; Rare:31 | ||||
| chr6:46922036-46922056 |