chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3180776186180776187TC40GENIChomozygous57820600
3180777411180777412GA57GENICpossibly homozygous57820602
3180778208180778209AG61GENIChomozygous57820604
3180781730180781731A-50GENIChomozygous57820608
3180782383180782384TC50GENIChomozygous57820610
3180782925180782926TC61GENIChomozygous57820612
3180783695180783707AGCCTGCTGCTT------------22GENIChomozygous57820614
3180784775180784776CT45GENIChomozygous57820616