Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:55534962-55535198 | Common:1; Rare:80 | ||||
chr5:55994888-55995152 | Rare:91 | ||||
chr5:56909476-56909627 | Common:1; Rare:41 | ||||
chr5:56952109-56952312 | Rare:74 | ||||
chr5:57173547-57173865 | Common:2; Rare:112 | ||||
chr5:58460063-58460241 | Common:4; Rare:70 | ||||
chr5:59768632-59768880 | Rare:60 | ||||
chr5:60945044-60945269 | Common:4; Rare:81; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr5:61162347-61162673 | Common:1; Rare:82 | ||||
chr5:62403856-62404032 | Common:3; Rare:58 | ||||
chr5:64768513-64768982 | Common:5; Rare:129 | ||||
chr5:65563116-65563308 | Common:3; Rare:67 | ||||
chr5:65624981-65625040 | Rare:17 | ||||
chr5:66144154-66144344 | Common:2; Rare:68 | ||||
chr5:67004055-67004355 | Common:3; Rare:97 |