| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43427454-43427580 | Rare:37 | ||||
| chr6:43516876-43517122 | Common:4; Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575962-43576234 | Common:1; Rare:112; Clinvar:8 | ||||
| chr6:43629164-43629462 | Common:2; Rare:86 | ||||
| chr6:43687663-43687912 | Common:2; Rare:91 | ||||
| chr6:43770081-43770235 | Common:2; Rare:47 | ||||
| chr6:43771181-43771253 | Common:1; Rare:36 | ||||
| chr6:43771812-43772022 | Rare:34 | ||||
| chr6:43772609-43772903 | Common:1; Rare:41 | ||||
| chr6:43773427-43773583 | Common:2; Rare:27 | ||||
| chr6:43776994-43777299 | Rare:56 | ||||
| chr6:44126711-44127052 | Common:1; Rare:85 | ||||
| chr6:44127276-44127669 | Common:4; Rare:109 | ||||
| chr6:44223447-44223821 | Common:2; Rare:110 | ||||
| chr6:44387407-44387789 | Common:4; Rare:97 |