chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121933089319330897CACG----11GENIChomozygous50614268
121933090719330908CT20GENIChomozygous50588071
121933094719330948TA34GENIChomozygous50098671
121933332819333329TC30GENIChomozygous50098673
121933402619334027AG34GENIChomozygous50098675
121933464219334643GGGTGT3GENICheterozygous50098679
121933464219334643GGGTGTGT3GENICheterozygous50597302
121933627119336272TC44GENIChomozygous50098683
121933756019337564GCCT----32GENIChomozygous50098685
121933893019338931TC26GENIChomozygous50098689
121933938019339381GC27GENIChomozygous50098691
121934023119340232GA47GENIChomozygous50098697
121934029119340292AG50GENIChomozygous50098699
121934129819341299AT37GENIChomozygous50098701
121934130019341301TG34GENIChomozygous50098703
121934137619341377GA46GENIChomozygous50098705
121934147719341478AG38GENIChomozygous50098707
121934212019342121CA39GENIChomozygous50098709
121934214519342147TG--33GENIChomozygous50098711
121934286319342864TTC33GENIChomozygous50098717
121934328819343289CT36GENIChomozygous50098719
121934441419344415GC43GENIChomozygous50098721
121934449719344498TC35GENIChomozygous50098723
121934455219344553G-27GENIChomozygous50098725
121934494419344946AC--45GENIChomozygous50098727