chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122373528123735282AT15GENIChomozygous115285640
122373580423735805TC33GENIChomozygous115285644
122373603623736037CT30GENIChomozygous115285646
122373627923736280TC15GENIChomozygous115285648
122373987423739875CT18GENIChomozygous115368572
122374050123740502AC20GENIChomozygous115368574
122374054123740542CT21GENIChomozygous115368576
122374167523741676TC15GENIChomozygous115285662
122374168623741687TC12GENIChomozygous115285664
122374192223741923GC6GENIChomozygous115368578
122374248123742482AG15GENIChomozygous115285666
122374249523742496CT16GENIChomozygous115285668
122374266823742669TC9GENIChomozygous115368580
122374270223742703GA5GENIChomozygous115368582
122374414423744145GA3GENIChomozygous115285670
122374520223745203GA9GENIChomozygous115368584
122374555923745560TC15GENIChomozygous115368586
122374560923745610CG8GENIChomozygous115285676
122374572223745723AC11GENIChomozygous115285678
122374593923745940GA17GENIChomozygous115368588
122374621523746216AG13GENIChomozygous115285680
122374710023747101TC8GENIChomozygous115505400
122374773223747733GC8GENIChomozygous115285686
122374784723747848CT22GENIChomozygous115368592
122374830823748309CT15GENIChomozygous115285688
122374883423748835TC15GENIChomozygous115285690
122374957223749573TC11GENIChomozygous115285692
122374970923749710CT14GENIChomozygous115368594
122375059023750591CT16GENIChomozygous115368596
122375072623750727CT5GENIChomozygous115368598
122375085523750856AG16GENIChomozygous115368600
122375085923750860GA15GENIChomozygous115368602
122375086823750869TC16GENIChomozygous115368604
122375195323751954AG14GENIChomozygous115285696
122375234623752347GT6GENIChomozygous115285698
122375255223752553GA10GENIChomozygous115368606