chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46580475165804752TC18GENICpossibly homozygous56926114
46580647765806478C-7GENIChomozygous56926116
46580724565807246TC15GENIChomozygous56926117
46580754865807554CCCACA------2GENIChomozygous56926118
46580834765808348TTG3GENIChomozygous56926120
46581408965814090AT16GENIChomozygous56926124
46581588865815889CT14GENICpossibly homozygous56926125
46581642865816429TC4GENICheterozygous56926126
46581782365817824TA14GENICpossibly homozygous56926128
46581787365817874GA16GENIChomozygous56926129