chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
63011885830118859CT120GENICheterozygous807661850
63011885930118860GA124GENICheterozygous807661851
63011887030118871GA138GENICheterozygous807661852
63011890530118906GT133GENICheterozygous807661853
63011891630118917GA129GENICheterozygous807661854
63011892830118929CG102GENICheterozygous807661855
63011892930118930AG117GENICheterozygous807661856
63016528730165288GA36GENIChomozygous807661857
63018827130188272CA16GENICpossibly homozygous807661858
63019598230195983TC37GENICpossibly homozygous807661859
63020832130208322GC17GENIChomozygous807661860
63020851530208516AG14GENIChomozygous807661861