chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5142692060142692061GT29GENICpossibly homozygous114033900
5142692740142692741TC30GENIChomozygous114033901
5142693278142693279GA29GENIChomozygous114343875
5142695901142695902TC31GENIChomozygous114033907