chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32406154424061545CA24GENIChomozygous111508023
32406196524061966AG20GENIChomozygous111508024
32406201324062014TC21GENIChomozygous111508025
32406202724062028AG23GENIChomozygous111508026
32406205024062051GA18GENIChomozygous111508027
32406322224063223GT15GENIChomozygous111508028
32406328724063288AG30GENICpossibly homozygous111508029
32406333724063338AG33GENICpossibly homozygous111508030
32406346924063470CT24GENIChomozygous111508031
32406349624063497TC16GENIChomozygous111508032
32406353424063535GA9GENICpossibly homozygous111508033
32406355224063553AG11GENIChomozygous111508034
32406362524063626AC14GENIChomozygous111508035
32406363324063634GA16GENIChomozygous111508036
32406381024063811AC17GENIChomozygous111508037
32406394924063950TC11GENIChomozygous111508038
32406437924064380TC6GENICheterozygous111508039
32406499524064996GA12GENICpossibly homozygous111508040
32406443524064436AC5GENIChomozygous111895707