| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43171054-43171524 | Rare:144 | ||||
| chr6:43182031-43182233 | Common:1; Rare:58 | ||||
| chr6:43427820-43427960 | Rare:46 | ||||
| chr6:43516712-43517169 | Common:6; Rare:169; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575939-43576185 | Rare:95; Clinvar:4 | ||||
| chr6:43770611-43770784 | Common:1; Rare:44; Clinvar:1 | ||||
| chr6:43771669-43771980 | Common:4; Rare:56 | ||||
| chr6:44126847-44126928 | Rare:21 | ||||
| chr6:44127331-44127681 | Common:4; Rare:101 | ||||
| chr6:44387448-44387736 | Common:4; Rare:73 | ||||
| chr6:44387757-44387849 | Rare:26 | ||||
| chr6:45328158-45328339 | Rare:46 | ||||
| chr6:45377424-45377696 | Common:4; Rare:93 | ||||
| chr6:45377769-45378129 | Common:2; Rare:112 | ||||
| chr6:45421996-45422088 | Rare:34 |