chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5145416825145416826CG19GENIChomozygous114038773
5145417108145417109CT9GENIChomozygous114038776
5145417551145417552CT15GENIChomozygous114038777
5145417910145417911CT23GENIChomozygous114038778
5145418030145418031GA20GENIChomozygous114038779
5145419932145419934GT14GENIChomozygous128250708
5145419974145419974TGTA19GENICpossibly homozygous128250709
5145420863145420864TC15GENIChomozygous114038780