chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174135186741351867GA6GENIChomozygous140923402
174135326841353269AC18GENICpossibly homozygous140116757
174135418641354187T17GENIChomozygous140022816
174135432341354324G18GENIChomozygous140022817
174135443641354437CT18GENIChomozygous140116758
174135510341355104CA21GENIChomozygous140116759
174135640041356400A24GENIChomozygous140022818
174135640741356408TA25GENIChomozygous140116760
174135720341357204CT18GENIChomozygous140116761
174135828241358283CT11GENIChomozygous140116762
174135888241358883AG25GENIChomozygous140116763
174135935941359360TG29GENIChomozygous140116764
174136154641361547AC23GENICpossibly homozygous140116765
174136168141361682CT18GENIChomozygous140116766
174136246241362463AT19GENIChomozygous140116767