chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3168601395168601396TA27GENIChomozygous141573082
3168601879168601880A18GENICpossibly homozygous141488142
3168603219168603220CT29GENIChomozygous141573083
3168610750168610751CT19GENIChomozygous141573084
3168608630168608630ATCTATCATTCTATTG18GENIChomozygous136601567
3168611504168611505AG25GENIChomozygous136860669
3168605877168605878GA26GENIChomozygous136860665
3168606907168606908GA21GENIChomozygous136860666
3168611296168611297AG27GENIChomozygous136860668
3168612024168612026AG26GENIChomozygous136601568
3168613895168613896T16GENICpossibly homozygous141488143
3168617307168617307TA9GENIChomozygous136601570