chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2106258813106258814AG30GENIChomozygous59000649
2106260186106260187AG30GENIChomozygous59000650
2106260835106260836AG30GENIChomozygous59000651
2106260866106260867TC34GENIChomozygous59000652
2106260932106260933GC31GENIChomozygous59000653
2106261605106261613ACACACAC--------13GENICheterozygous59000654
2106261607106261613ACACAC------13GENICpossibly homozygous60128086