chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3180775961180775962GT38GENICpossibly homozygous58266269
3180776186180776187TC29GENIChomozygous57820600
3180777411180777412GA24GENICpossibly homozygous57820602
3180778208180778209AG26GENIChomozygous57820604
3180778223180778224GA22GENIChomozygous58266271
3180782166180782167CT40GENIChomozygous58266274
3180782383180782384TC37GENIChomozygous57820610
3180782925180782926TC31GENIChomozygous57820612
3180782938180782939GA37GENIChomozygous58266276
3180783695180783707AGCCTGCTGCTT------------11GENIChomozygous57820614
3180784775180784776CT34GENIChomozygous57820616
3180784914180784915GA31GENIChomozygous58266278