| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42879577-42879934 | Rare:105 | ||||
| chr6:42890786-42890973 | Rare:69 | ||||
| chr6:42929209-42929571 | Common:4; Rare:108 | ||||
| chr6:42984307-42984638 | Rare:87 | ||||
| chr6:43013822-43014327 | Common:2; Rare:125 | ||||
| chr6:43516861-43517127 | Common:4; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575933-43576186 | Common:1; Rare:97; Clinvar:4 | ||||
| chr6:43635697-43635893 | Common:2; Rare:45 | ||||
| chr6:43687757-43687860 | Common:1; Rare:42 | ||||
| chr6:43770081-43770221 | Common:2; Rare:42 | ||||
| chr6:44127348-44127652 | Common:4; Rare:90 | ||||
| chr6:44219496-44219661 | Common:1; Rare:41 | ||||
| chr6:44223489-44223618 | Common:1; Rare:45 | ||||
| chr6:44246904-44247179 | Common:4; Rare:114 | ||||
| chr6:44257480-44257673 | Rare:55 |