| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43182137-43182235 | Rare:30 | ||||
| chr6:43308401-43308427 | Rare:3 | ||||
| chr6:43427411-43427572 | Rare:39 | ||||
| chr6:43427783-43427925 | Rare:42 | ||||
| chr6:43516782-43517115 | Common:6; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575957-43576234 | Common:1; Rare:115; Clinvar:8 | ||||
| chr6:43687718-43687860 | Common:1; Rare:56 | ||||
| chr6:43687923-43688113 | Common:1; Rare:37 | ||||
| chr6:43770081-43770316 | Common:4; Rare:65 | ||||
| chr6:43770620-43770784 | Rare:43 | ||||
| chr6:43771660-43771996 | Common:4; Rare:60 | ||||
| chr6:43772806-43773042 | Common:1; Rare:35 | ||||
| chr6:43773424-43773597 | Common:2; Rare:29 | ||||
| chr6:43774202-43774412 | Rare:54 | ||||
| chr6:44127278-44127677 | Common:4; Rare:112 |