chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
62126440621264407TA20GENIChomozygous54862703
62126443321264434AG14GENIChomozygous54862704
62126495321264954GGCA9GENIChomozygous54862705
62126573221265733AT7GENICheterozygous54862707
62126578721265788AG2GENIChomozygous54862708
62126650221266503GC16GENIChomozygous54862709
62126774221267743GA4GENIChomozygous54862710
62126856421268565AG16GENICpossibly homozygous54862711
62126886021268861AG3GENIChomozygous54862712
62126924221269243GGT2GENIChomozygous54294157
62127094721270948T-10GENIChomozygous54294159
62127246721272468CT10GENICpossibly homozygous54862713
62127387121273872AG12GENIChomozygous54862714
62127536121275362GA9GENIChomozygous54862715
62127617721276178CT9GENICheterozygous54862716
62127830721278308GT2GENIChomozygous54862717
62127835021278351CCA1GENIChomozygous54294162
62127963521279636GA2GENIChomozygous54862719
62127977821279779TC1GENIChomozygous54862721