chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5117878339117878340CT65GENIChomozygous137598756
5117878843117878843TTTGT59GENIChomozygous137335922
5117881801117881802TG38GENIChomozygous137598757
5117884262117884262A59GENICpossibly homozygous137335923
5117885727117885728GA54GENIChomozygous137598758
5117886726117886727AG57GENIChomozygous137598759
5117887761117887762CA67GENICpossibly homozygous137598760
5117888585117888586GA58GENIChomozygous137598761
5117890655117890655TTT65GENIChomozygous137335924
5117893938117893939AC61GENIChomozygous137598762
5117893963117893964AC55GENIChomozygous137598763
5117894576117894577TC61GENIChomozygous137598764
5117895878117895879TG59GENICpossibly homozygous137598765
5117896044117896045TG59GENIChomozygous137598766
5117896117117896118AG52GENIChomozygous137598767
5117896817117896818GA55GENIChomozygous137598768
5117901914117901915A46GENICpossibly homozygous137335925
5117902462117902463CT67GENIChomozygous137598769
5117903341117903342GA56GENIChomozygous137598770
5117905631117905632TA54GENIChomozygous137598771
5117909028117909029AG45GENIChomozygous137598772
5117911631117911632AG45GENIChomozygous137598773
5117912754117912755TC48GENIChomozygous137598774
5117918644117918645AT62GENIChomozygous137598775
5117920132117920133T45GENICpossibly homozygous137335926
5117921709117921710CT51GENIChomozygous137598776