| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42929209-42929556 | Common:4; Rare:97 | ||||
| chr6:42984284-42984635 | Rare:91 | ||||
| chr6:43013869-43014323 | Common:2; Rare:100 | ||||
| chr6:43308796-43308978 | Common:1; Rare:53 | ||||
| chr6:43516850-43517115 | Common:5; Rare:97; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575911-43576234 | Common:2; Rare:128; Clinvar:8 | ||||
| chr6:43687768-43687823 | Common:1; Rare:22 | ||||
| chr6:43770087-43770242 | Common:2; Rare:48 | ||||
| chr6:43771896-43772022 | Rare:22 | ||||
| chr6:44127334-44127677 | Common:4; Rare:100 | ||||
| chr6:44219453-44219645 | Rare:47 | ||||
| chr6:44223441-44223626 | Common:1; Rare:56 | ||||
| chr6:44246880-44247193 | Common:4; Rare:132 | ||||
| chr6:44387407-44387747 | Common:4; Rare:84 | ||||
| chr6:45377860-45378189 | Common:2; Rare:113 |