Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45507228-45507535 | Common:1; Rare:84 | ||||
chr19:45692373-45692713 | Common:1; Rare:79 | ||||
chr19:46601147-46601420 | Common:3; Rare:81; Clinvar (benign):1 | ||||
chr19:46608290-46608487 | Common:1; Rare:53; Clinvar (benign):4 | ||||
chr19:47256472-47256568 | Rare:33 | ||||
chr19:47484242-47484307 | Common:1; Rare:16 | ||||
chr19:48170259-48170669 | Common:2; Rare:115 | ||||
chr19:48390887-48390962 | Rare:7 | ||||
chr19:48619139-48619428 | Rare:92 | ||||
chr19:48965461-48965916 | Common:1; Rare:166; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr19:48993253-48993484 | Common:2; Rare:111; Clinvar:3; Clinvar (benign):2 | ||||
chr19:49496108-49496476 | Common:1; Rare:125 | ||||
chr19:49527769-49528033 | Common:4; Rare:84 | ||||
chr19:49665750-49666029 | Common:3; Rare:135; Clinvar (pathogenic):1 | ||||
chr19:49867531-49867646 | Common:2; Rare:37 |