Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:55298447-55298730 | Common:3; Rare:44 | ||||
chr2:57194193-57194241 | Rare:14 | ||||
chr2:57195653-57195802 | Common:4; Rare:38 | ||||
chr2:57227421-57227540 | Common:3; Rare:49 | ||||
chr2:58160168-58160200 | Rare:9; Clinvar (benign):1 | ||||
chr2:58428151-58428459 | Common:3; Rare:91 | ||||
chr2:60419786-60419902 | Rare:22 | ||||
chr2:61186216-61186497 | Common:1; Rare:95 | ||||
chr2:61190579-61190716 | Rare:49 | ||||
chr2:61508922-61508937 | Rare:4 | ||||
chr2:61871898-61872087 | Common:1; Rare:44 | ||||
chr2:62880976-62881262 | Common:3; Rare:47 | ||||
chr2:63187618-63187691 | Rare:15 | ||||
chr2:63598923-63599292 | Common:1; Rare:66 | ||||
chr2:63604417-63604828 | Common:2; Rare:84 |