Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:18279526-18279820 | Rare:105 | ||||
chr19:18519263-18519449 | Rare:31 | ||||
chr19:23762855-23763011 | Common:1; Rare:52 | ||||
chr19:33300514-33300725 | Common:1; Rare:44 | ||||
chr19:35887305-35887540 | Rare:42 | ||||
chr19:35889814-35889892 | Rare:32 | ||||
chr19:35898929-35899159 | Rare:41 | ||||
chr19:35903609-35903763 | Rare:32 | ||||
chr19:35909277-35909742 | Common:2; Rare:105 | ||||
chr19:36125495-36125711 | Rare:68 | ||||
chr19:36142909-36143129 | Rare:55 | ||||
chr19:39403698-39404097 | Rare:80 | ||||
chr19:39410361-39411019 | Common:5; Rare:125 | ||||
chr19:39411454-39411620 | Common:1; Rare:33 | ||||
chr19:41331924-41332185 | Rare:59; Clinvar (benign):1 |