chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2106258813106258814AG46GENICpossibly homozygous59000649
2106260186106260187AG46GENIChomozygous59000650
2106260835106260836AG46GENIChomozygous59000651
2106260866106260867TC42GENIChomozygous59000652
2106260932106260933GC48GENIChomozygous59000653
2106261607106261613ACACAC------30GENIChomozygous60128086