chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
205109676051096761A-11GENICpossibly homozygous704630769
205109686451096867GTC---29GENIChomozygous704630770
205109727051097271GA31GENIChomozygous557422935
205109852751098528AC25GENIChomozygous557422936
205109854451098545TC23GENIChomozygous557422937
205109895051098951TG11GENIChomozygous558043373
205109976651099767TC25GENIChomozygous557422938
205109989051099891GT28GENIChomozygous557422939
205110026051100261TC29GENIChomozygous557422940
205110169651101697TC22GENIChomozygous557422941
205110209351102094GA32GENIChomozygous557422942
205110234551102346CT28GENIChomozygous558043374
205110242351102424GA26GENIChomozygous558043375
205110254251102543CT38GENIChomozygous557422943
205110536851105395AAGAAGAAGAAGAAGAAGAAGAAGAAG---------------------------11GENIChomozygous704630771
205110586751105868AAATAT1GENIChomozygous704630773
205110646051106461AC32GENIChomozygous557422944
205110661651106617AAT20GENIChomozygous704630775
205110661951106626CAACAAC-------18GENIChomozygous704630776
205110673251106733CT20GENIChomozygous557422945
205110680451106805AG26GENIChomozygous557422946
205110687451106875TC20GENIChomozygous557422947
205110766151107662A-9GENICheterozygous704630777
205110790851107909CCAAAA3GENICheterozygous704630778
205110937351109374TTA8GENIChomozygous704630780
205110996551109966T-22GENIChomozygous704630782
205111104251111043GA23GENIChomozygous558043376
205111222451112225GA29GENIChomozygous557422948
205111238051112381CG31GENIChomozygous557422949
205111377851113779A-11GENIChomozygous704630784
205111405951114060CT9GENIChomozygous558043377
205111452351114525TC--2GENICheterozygous704630785
205111568951115690GA22GENIChomozygous558043378
205111713451117135A-6GENIChomozygous704630789
205111776951117770GGA16GENIChomozygous704630791
205111786451117865GA9GENIChomozygous557422950
205111789651117899AAG---8GENIChomozygous704630793