chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148262241782622419CT--3GENIChomozygous49439417
148262337482623375TC29GENIChomozygous49016969
148262561182625612AG39GENIChomozygous49016970
148262726682627282GTGTGTGTGTGTGTGT----------------8GENIChomozygous49431009
148263524382635251ATACATAC--------7GENIChomozygous49431010
148263592082635921CCA17GENICpossibly homozygous49016972
148263696882636969GA23GENIChomozygous49016973
148264079182640793TT--11GENIChomozygous49347176
148264079482640795TC10GENICpossibly homozygous49347177
148264320482643205AAT4GENICheterozygous49331990
148264426182644277AGAGAGAGAGAGAGAG----------------9GENIChomozygous49431012
148264762482647625TC27GENIChomozygous49016975
148264855282648553CCT6GENIChomozygous49016976
148265252482652525CT31GENIChomozygous49016977
148265288582652886TG16GENICpossibly homozygous49016978
148265600782656008T-15GENICheterozygous49327526
148265785882657859TTC15GENICpossibly homozygous49016979
148265886782658868CCAG9GENIChomozygous49431013
148265887382658874CCAG11GENIChomozygous49431014