Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:52139877-52140173 | Common:3; Rare:81 | ||||
chr19:52369851-52369950 | Rare:31 | ||||
chr19:52397691-52397898 | Common:5; Rare:66 | ||||
chr19:52735016-52735227 | Common:5; Rare:65 | ||||
chr19:53254808-53255011 | Common:1; Rare:70 | ||||
chr19:53866347-53866410 | Common:1; Rare:17 | ||||
chr19:53867833-53867941 | Rare:22 | ||||
chr19:54115289-54115434 | Common:1; Rare:34; Clinvar (benign):1 | ||||
chr19:54115628-54115787 | Common:1; Rare:38; Clinvar:4 | ||||
chr19:54159678-54159739 | Rare:28 | ||||
chr19:54159741-54160085 | Rare:108 | ||||
chr19:54200696-54200891 | Common:2; Rare:74 | ||||
chr19:54449018-54449249 | Common:3; Rare:66 | ||||
chr19:54966251-54966405 | Common:2; Rare:43 | ||||
chr19:55385759-55385978 | Common:6; Rare:73 |