chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122052009820520099AG11GENIChomozygous50105508
122052061520520616TC30GENICpossibly homozygous50105510
122052123120521232TG29GENIChomozygous50105512
122052238220522383CT9GENIChomozygous50105514
122052265520522658GGG---4GENIChomozygous50105516
122052266220522663GT4GENIChomozygous50507605
122052286220522863CT1GENIChomozygous50105518
122052376820523769TC10GENIChomozygous50105520
122052528820525289TC8GENIChomozygous50105522
122052713020527131TC9GENIChomozygous50105524