chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1256102280256102281TC27GENIChomozygous108620034
1256102399256102400CT33GENIChomozygous108620036
1256104172256104173CT60GENIChomozygous108620038
1256104389256104390TC51GENIChomozygous108620040
1256104523256104524TC39GENICpossibly homozygous108620042
1256104713256104714AC51GENIChomozygous108620044
1256104958256104959AG35GENIChomozygous108620046
1256104985256104986GA32GENIChomozygous108620048
1256105186256105187AC34GENIChomozygous108620050
1256105539256105540AG25GENIChomozygous108620052
1256105554256105555CT20GENIChomozygous108620054
1256106108256106109CT25GENICpossibly homozygous108620055
1256106383256106384CT28GENIChomozygous108620057
1256107227256107228CT54GENIChomozygous108620059