chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122052009820520099AG27GENIChomozygous50105508
122052061520520616TC26GENIChomozygous50105510
122052123120521232TG38GENIChomozygous50105512
122052238220522383CT42GENIChomozygous50105514
122052265520522658GGG---54GENIChomozygous50105516
122052266220522663GT55GENIChomozygous50507605
122052286220522863CT69GENICpossibly homozygous50105518
122052376820523769TC74GENIChomozygous50105520
122052528820525289TC64GENIChomozygous50105522
122052713020527131TC52GENIChomozygous50105524