chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1256102649256102660GGGCCCCGGGA26GENIChomozygous131266879
1256103656256103657GA25GENIChomozygous120605096
1256104172256104173CT20GENIChomozygous108620038
1256104389256104390TC17GENIChomozygous108620040
1256104523256104524TC23GENIChomozygous108620042
1256104713256104714AC18GENIChomozygous108620044
1256104958256104959AG15GENIChomozygous108620046
1256105539256105540AG23GENICpossibly homozygous108620052
1256105554256105555CT24GENIChomozygous108620054
1256105576256105578AA26GENIChomozygous127505334
1256105621256105631TAGCTTCCTG23GENIChomozygous127505335
1256106108256106109CT22GENICpossibly homozygous108620055
1256106966256106967TG28GENIChomozygous120605098
1256107147256107148CT23GENIChomozygous109376206
1256107227256107228CT26GENIChomozygous108620059
1256107548256107549T27GENIChomozygous127505336