chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13103396387103396388GA15GENIChomozygous49872385
13103396689103396690AG17GENIChomozygous49872386
13103396962103396963A-9GENIChomozygous49872387
13103398351103398352AG12GENIChomozygous49872388
13103400011103400012AG7GENIChomozygous49872390
13103400922103400923TC11GENIChomozygous49872391
13103401882103401883AG16GENICpossibly homozygous49872392
13103402340103402341CA1GENIChomozygous50628021
13103403084103403085TC12GENIChomozygous49872401
13103403525103403526TG19GENIChomozygous49872402
13103404007103404008AG11GENIChomozygous49872403
13103404191103404192TA3GENICheterozygous49872404
13103404201103404202AG6GENIChomozygous49872405
13103404532103404533CT11GENIChomozygous49872406
13103404933103404934CCACACACACACACACACACACACAT5GENICheterozygous50597261
13103405017103405018GT9GENICpossibly homozygous49872407
13103405090103405091TTAG8GENIChomozygous49872408
13103405468103405469GA16GENIChomozygous49872409
13103405818103405819TA18GENICpossibly homozygous49872412
13103406234103406235TC12GENICpossibly homozygous49872413
13103406524103406525TC9GENIChomozygous49872414