chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109016585290165853TTC10GENIChomozygous51537795
109016586190165862TTTG7GENIChomozygous51537796
109016644790166448AAT19GENICpossibly homozygous51537797
109016739590167396GA30GENIChomozygous51736004
109016797990167980CT39GENIChomozygous51537798
109016857790168578TC21GENIChomozygous51537799
109017161090171611CA34GENIChomozygous51537800