chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145777453145777454TC30GENIChomozygous56968704
4145780831145780833TC--15GENIChomozygous56968705
4145780977145780978CA27GENIChomozygous56968707
4145781127145781128TTAC22GENICheterozygous56968708
4145781127145781128TTACAC22GENICpossibly homozygous56968710
4145781159145781160AACACAC22GENIChomozygous56968712
4145781239145781240TTACACACAC8GENICheterozygous58469508
4145781239145781240TTACACAC8GENICheterozygous58344237
4145781239145781240TTACACACACACACACACAC8GENICheterozygous58344239
4145783050145783051GA32GENIChomozygous56968716
4145783174145783175GA34GENIChomozygous56968717
4145783649145783650AG29GENIChomozygous56968719
4145783800145783801CT50GENIChomozygous56968720
4145784855145784856GA27GENIChomozygous56968722
4145784948145784949AG36GENIChomozygous56968723