chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122992253229922533CT22GENICpossibly homozygous50167719
122992423629924237AG15GENIChomozygous50167721
122992433929924340AG27GENIChomozygous50167723
122992530329925304CG25GENICpossibly homozygous50167725
122992570129925702CG20GENICpossibly homozygous50167727
122992585329925854GA20GENICpossibly homozygous50167729
122992623729926238A-18GENICpossibly homozygous50167731
122992630129926302CT16GENIChomozygous50167733
122992665229926653C-2GENIChomozygous50167737
122992747529927476T-13GENICheterozygous50167741
122992765429927655CT20GENIChomozygous50167743
122992779429927795AT19GENIChomozygous50167745
122992932929929330CT15GENICpossibly homozygous50167747
122993033729930338AG16GENICpossibly homozygous50167749