chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1420852762085277TC11GENIChomozygous113316830
1420856472085648GA9GENIChomozygous113316832
1420863762086377AG24GENIChomozygous113316833
1420863972086398CT27GENIChomozygous113316834
1420871242087125CT20GENIChomozygous113316835
1420876762087677GT27GENICpossibly homozygous113316836
1420884082088409TC17GENIChomozygous113316837
1420894072089408AT21GENIChomozygous113316838
1420894132089414TA22GENIChomozygous113316839
1420894372089438TG26GENIChomozygous113316840
1420902602090261GA11GENIChomozygous113316841
1420914712091472TG16GENIChomozygous113316842
1420916452091646CT14GENIChomozygous113316843
1420928182092819TC19GENIChomozygous113316844
1420942442094245AC20GENIChomozygous113316845
1420949522094953GA24GENIChomozygous113316846
1420951522095153CT21GENIChomozygous113316847
1420955862095587AG20GENIChomozygous113316848
1420956612095662CT13GENIChomozygous113316849
1420980422098043TC10GENIChomozygous113316850
1420982862098287CT22GENIChomozygous113316851