| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:58046609-58046672 | Rare:18 | ||||
| chr2:58046675-58046845 | Rare:51 | ||||
| chr2:58047224-58047269 | Rare:15 | ||||
| chr2:58241309-58241431 | Rare:66; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:60881307-60881664 | Common:2; Rare:135 | ||||
| chr2:61017434-61017784 | Common:1; Rare:113; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:61144921-61145165 | Common:3; Rare:82 | ||||
| chr2:61162074-61162198 | Rare:21 | ||||
| chr2:61177197-61177458 | Common:5; Rare:110 | ||||
| chr2:61471167-61471392 | Common:4; Rare:87 | ||||
| chr2:61854021-61854081 | Common:1; Rare:24; Clinvar:1 | ||||
| chr2:61888564-61888693 | Common:1; Rare:55 | ||||
| chr2:62506167-62506330 | Common:1; Rare:57 | ||||
| chr2:63588250-63588546 | Common:1; Rare:85; Clinvar:6 | ||||
| chr2:63588683-63589025 | Rare:110 |