chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122373528123735282AT14GENIChomozygous115285640
122373571123735712TC16GENIChomozygous115469736
122373580423735805TC12GENIChomozygous115285644
122373603623736037CT13GENIChomozygous115285646
122373627923736280TC11GENIChomozygous115285648
122374069223740693CA8GENIChomozygous115469738
122374167523741676TC9GENIChomozygous115285662
122374168623741687TC7GENIChomozygous115285664
122374248123742482AG13GENIChomozygous115285666
122374249523742496CT16GENIChomozygous115285668
122374266823742669TC10GENIChomozygous115368580
122373987423739875CT19GENIChomozygous115368572
122374050123740502AC12GENIChomozygous115368574
122374054123740542CT14GENIChomozygous115368576
122374192223741923GC10GENIChomozygous115368578
122374270223742703GA16GENIChomozygous115368582
122374414423744145GA10GENIChomozygous115285670
122374520223745203GA18GENIChomozygous115368584
122374555923745560TC15GENIChomozygous115368586
122374560923745610CG14GENIChomozygous115285676
122374572223745723AC5GENIChomozygous115285678
122374593923745940GA15GENIChomozygous115368588
122374621523746216AG6GENIChomozygous115285680
122374737023747371GT19GENIChomozygous115285684
122374773223747733GC5GENIChomozygous115285686
122374784723747848CT13GENIChomozygous115368592
122374830823748309CT19GENIChomozygous115285688
122374883423748835TC10GENIChomozygous115285690
122374957223749573TC25GENIChomozygous115285692
122374970923749710CT13GENIChomozygous115368594
122375059023750591CT16GENIChomozygous115368596
122375072623750727CT20GENIChomozygous115368598
122375195323751954AG10GENIChomozygous115285696
122375234623752347GT24GENIChomozygous115285698
122375255223752553GA19GENIChomozygous115368606
122374579523745796TC7GENIChomozygous126224021
122374796823747969AG10GENICheterozygous126170845