chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171041176910411770CG29GENIChomozygous110953988
171041227410412275TA36GENIChomozygous110953990
171041256210412563GC37GENIChomozygous110953992
171041363910413640TG18GENICpossibly homozygous110953994
171041388710413888AG29GENICpossibly homozygous110953996
171041439910414400TC30GENIChomozygous110953998