Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:52297052-52297198 | Common:18; Rare:38 | ||||
chr19:52369851-52369952 | Rare:33 | ||||
chr19:52397733-52397890 | Common:4; Rare:48 | ||||
chr19:52857588-52857745 | Common:4; Rare:45 | ||||
chr19:53254833-53255042 | Common:2; Rare:71 | ||||
chr19:53365522-53365752 | Common:6; Rare:62 | ||||
chr19:54102674-54102887 | Common:3; Rare:56 | ||||
chr19:54115273-54115484 | Common:2; Rare:56; Clinvar (benign):2 | ||||
chr19:54115628-54115797 | Common:1; Rare:43; Clinvar:4 | ||||
chr19:54189328-54189448 | Common:1; Rare:36 | ||||
chr19:54200728-54200891 | Common:2; Rare:62 | ||||
chr19:54449045-54449229 | Common:2; Rare:52 | ||||
chr19:55385879-55385968 | Common:2; Rare:41 | ||||
chr19:56314828-56314927 | Common:1; Rare:31 | ||||
chr19:56368248-56368347 | Common:2; Rare:31 |