chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145777453145777454TC54GENIChomozygous56968704
4145780831145780833TC--46GENIChomozygous56968705
4145780977145780978CA48GENIChomozygous56968707
4145781127145781128TTAC3GENIChomozygous56968708
4145781159145781160AACACAC7GENICpossibly homozygous56968712
4145781205145781206T-9GENICheterozygous56968713
4145781216145781219ATA---9GENICheterozygous57343962
4145783050145783051GA54GENICpossibly homozygous56968716
4145783174145783175GA35GENIChomozygous56968717
4145783649145783650AG68GENIChomozygous56968719
4145783800145783801CT61GENIChomozygous56968720
4145784855145784856GA60GENIChomozygous56968722
4145784948145784949AG51GENIChomozygous56968723