| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43013793-43014339 | Common:2; Rare:137 | ||||
| chr6:43308801-43308915 | Rare:43 | ||||
| chr6:43427431-43427603 | Rare:44 | ||||
| chr6:43427783-43427915 | Rare:34 | ||||
| chr6:43477488-43477596 | Rare:24 | ||||
| chr6:43516771-43517130 | Common:6; Rare:132; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575952-43576224 | Common:1; Rare:113; Clinvar:7 | ||||
| chr6:43635740-43635894 | Common:1; Rare:41 | ||||
| chr6:43644995-43645204 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr6:43687744-43687853 | Common:1; Rare:49 | ||||
| chr6:43770081-43770267 | Common:3; Rare:54 | ||||
| chr6:43771847-43771996 | Rare:28 | ||||
| chr6:44127278-44127678 | Common:4; Rare:112 | ||||
| chr6:44223258-44223615 | Common:1; Rare:84 | ||||
| chr6:44246083-44246217 | Rare:31 |