chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108903385289033853TC69GENIChomozygous116819476
108903439389034394AG64GENIChomozygous116674984
108903512789035128GT44GENIChomozygous116674986
108903541689035417AG60GENIChomozygous116674988
108903554089035541GA54GENIChomozygous117020483
108903639489036395TC82GENICheterozygous118069441
108903566189035664GCG64GENICpossibly homozygous128843586
108903566989035669GG67GENICpossibly homozygous128843587
108903599989036000GA73GENIChomozygous117346812