chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2234575769234575770T-12GENIChomozygous59446741
2234577655234577656CT23GENIChomozygous59942481
2234578714234578715T-18GENIChomozygous59446744
2234579280234579281TA18GENIChomozygous59942482
2234579389234579391AA--6GENICheterozygous59446746
2234579390234579391A-6GENICheterozygous59446747
2234579618234579619C-27GENIChomozygous59446749
2234580111234580112CT24GENIChomozygous59446750
2234580468234580469GA23GENIChomozygous59942483
2234581524234581525A-29GENIChomozygous59446751
2234581790234581791GGTGAATGAA17GENICpossibly homozygous59446752
2234581790234581791GGTGAA17GENICheterozygous59776455
2234583049234583050AG28GENIChomozygous59942484
2234583933234583934A-12GENICpossibly homozygous59776456
2234584077234584078TC20GENIChomozygous59446755
2234593885234593886CT22GENIChomozygous59942485
2234594642234594643A-16GENIChomozygous59446760
2234596398234596399TTA11GENICpossibly homozygous59942486
2234597723234597724AG22GENIChomozygous59446764
2234598310234598316ACACAC------5GENICheterozygous61601949
2234598312234598316ACAC----5GENICheterozygous61538654
2234600509234600510A-16GENIChomozygous59446770
2234601347234601351TGGG----20GENIChomozygous60551108
2234601351234601352TTCCC20GENIChomozygous60551109
2234602197234602198AC20GENIChomozygous59942488
2234602480234602481CT22GENIChomozygous59942489
2234602493234602494CA24GENIChomozygous60247864
2234602629234602630GGA23GENIChomozygous59446775
2234603144234603145CT28GENIChomozygous59942490