chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1162370053162370054GC50GENIChomozygous108344449
1162371170162371171AT43GENIChomozygous108344451
1162372300162372301AG54GENIChomozygous108344453
1162372421162372422GA57GENIChomozygous108344455
1162372501162372502CT43GENIChomozygous108344457
1162372880162372881AC53GENIChomozygous108344459
1162373507162373508AG45GENIChomozygous108344461
1162373838162373839AT48GENIChomozygous108344463
1162373987162373988AG48GENIChomozygous108344465
1162374382162374383TC58GENIChomozygous108344467
1162374592162374593CG71GENIChomozygous108344469
1162374767162374768GA50GENIChomozygous108344471
1162374912162374913CG37GENIChomozygous108344473
1162374945162374946GA28GENIChomozygous108344475
1162374966162374967AG17GENIChomozygous108344477
1162375025162375026AG31GENIChomozygous108344479
1162375342162375343AG33GENIChomozygous108344481
1162375364162375365AC30GENIChomozygous108751119
1162373097162373097GTTG32GENIChomozygous127451447
1162373615162373616T54GENIChomozygous127451448
1162374819162374820CT48GENIChomozygous108751116
1162374820162374821TG50GENIChomozygous108751117
1162375363162375364GA31GENIChomozygous108751118
1162375683162375684TC49GENIChomozygous108344483