chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122608934626089347TTTGCTC4GENIChomozygous50145578
122608935626089357CA7GENIChomozygous50145580
122608965026089651AG19GENIChomozygous50145582
122609002226090023GA23GENIChomozygous50145584
122609004226090043GA18GENIChomozygous50145586
122609020226090203CG15GENIChomozygous50145588
122609056326090564AC21GENICpossibly homozygous50145590
122609207426092075AG5GENICheterozygous50372917
122609514926095150GGAA4GENICheterozygous50145593
122609601326096014CT21GENICpossibly homozygous50145597