chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5100925544100925545TA69GENIChomozygous113939963
5100925578100925579GT87GENIChomozygous113939964
5100925691100925692CT84GENIChomozygous113939965
5100926918100926919AT52GENIChomozygous113939966
5100931682100931683CG78GENICpossibly homozygous113939967
5100932061100932062CT61GENIChomozygous113939968
5100933273100933274CG39GENIChomozygous113939969
5100939518100939519AG50GENIChomozygous113939970
5100942181100942182GA70GENIChomozygous113939971
5100942190100942191AG67GENIChomozygous113939972
5100946159100946160CT43GENIChomozygous113939973
5100950412100950413AG84GENICheterozygous113939975
5100951810100951811TC69GENIChomozygous113939976
5100952747100952748AT87GENIChomozygous113939977
5100963919100963920GT66GENIChomozygous113939978
5100971867100971868AG47GENIChomozygous113939979
5100976218100976219GA10GENIChomozygous113939980
5100976224100976225AG8GENIChomozygous113939981