| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43013852-43014329 | Common:2; Rare:112 | ||||
| chr6:43040720-43040925 | Rare:53 | ||||
| chr6:43076123-43076468 | Rare:109 | ||||
| chr6:43427284-43427580 | Common:1; Rare:59 | ||||
| chr6:43477493-43477589 | Rare:19 | ||||
| chr6:43516887-43517127 | Common:4; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575962-43576224 | Common:1; Rare:108; Clinvar:7 | ||||
| chr6:43635740-43635894 | Common:1; Rare:41 | ||||
| chr6:43770088-43770230 | Common:2; Rare:43 | ||||
| chr6:44127369-44127669 | Common:4; Rare:86 | ||||
| chr6:44387610-44387738 | Common:2; Rare:39 | ||||
| chr6:45421977-45422116 | Common:1; Rare:46 | ||||
| chr6:46129777-46130071 | Common:5; Rare:91 | ||||
| chr6:46652667-46653013 | Rare:83 | ||||
| chr6:47477695-47478242 | Common:5; Rare:159; Clinvar:7; Clinvar (benign):7 |