| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42890789-42890870 | Rare:39 | ||||
| chr6:42929206-42929581 | Common:4; Rare:113 | ||||
| chr6:42984307-42984629 | Rare:81 | ||||
| chr6:43013809-43014313 | Common:2; Rare:128 | ||||
| chr6:43053879-43053989 | Common:1; Rare:31; Clinvar:4 | ||||
| chr6:43076166-43076467 | Rare:95 | ||||
| chr6:43427461-43427576 | Rare:34 | ||||
| chr6:43477333-43477589 | Common:2; Rare:49 | ||||
| chr6:43516828-43517112 | Common:5; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575903-43576227 | Common:2; Rare:132; Clinvar:8 | ||||
| chr6:43687765-43687868 | Common:1; Rare:43 | ||||
| chr6:43770081-43770230 | Common:2; Rare:45 | ||||
| chr6:44127351-44127669 | Common:4; Rare:92 | ||||
| chr6:44223453-44223615 | Common:1; Rare:49 | ||||
| chr6:44246913-44247193 | Common:4; Rare:118 |