chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122417223524172236AATGGTCCTGCC10GENIChomozygous50589132
122417319124173192CT16GENIChomozygous50131987
122417481424174815TTGTGC12GENIChomozygous50607900
122417496524174966AAGT21GENIChomozygous50131997
122417501524175016TTGTGTGTGA14GENIChomozygous50132001
122417503924175041GT--13GENIChomozygous50589133
122417505224175053TA15GENIChomozygous50589134
122417541724175418CA16GENIChomozygous50589135
122417547024175471CT21GENIChomozygous50292660
122417624924176253TCCA----5GENIChomozygous50607901
122417669224176693GA17GENIChomozygous50589136
122417669824176699GT16GENIChomozygous50292665
122417682424176825AG12GENIChomozygous50132021