chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1162370053162370054GC20GENIChomozygous108344449
1162371170162371171AT22GENIChomozygous108344451
1162372300162372301AG19GENICpossibly homozygous108344453
1162372421162372422GA33GENIChomozygous108344455
1162372501162372502CT29GENIChomozygous108344457
1162372880162372881AC28GENIChomozygous108344459
1162373507162373508AG24GENIChomozygous108344461
1162373838162373839AT22GENIChomozygous108344463
1162373987162373988AG26GENIChomozygous108344465
1162374382162374383TC18GENIChomozygous108344467
1162374592162374593CG17GENIChomozygous108344469
1162374767162374768GA26GENIChomozygous108344471
1162374819162374820CT25GENIChomozygous108751116
1162374820162374821TG25GENIChomozygous108751117
1162374912162374913CG17GENIChomozygous108344473
1162374945162374946GA16GENIChomozygous108344475
1162375025162375026AG10GENIChomozygous108344479
1162375342162375343AG23GENIChomozygous108344481
1162375363162375364GA23GENIChomozygous108751118
1162375364162375365AC23GENIChomozygous108751119
1162375683162375684TC21GENIChomozygous108344483