chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71225975312259754GA19GENIChomozygous115569716
71226097212260973CT21GENIChomozygous115569717
71226100412261005CT25GENIChomozygous115569718
71226141912261420GT19GENIChomozygous115569719
71226142612261427AG19GENIChomozygous115569720
71226172912261730CT36GENIChomozygous115569721
71226234712262348GA23GENIChomozygous115569722
71226415212264153CT27GENIChomozygous115569723
71226416912264170GA26GENIChomozygous115569724
71226501812265019AG31GENIChomozygous115569725
71226721012267210A17GENIChomozygous128435699
71226756612267567GT28GENIChomozygous115569726
71227088612270887GA26GENIChomozygous115569727
71227127512271276TC28GENIChomozygous115569728
71227199212271993G19GENIChomozygous128435700
71227261312272614T22GENIChomozygous128435701
71227310212273110TCTGAGTT22GENIChomozygous128435702
71227322912273230TC15GENIChomozygous115569729
71227354912273550T17GENIChomozygous128435703
71227381012273811CG21GENIChomozygous115569730
71227404712274047GGTG16GENIChomozygous128435704
71227455112274552TG31GENIChomozygous115569731
71227487212274873AG24GENIChomozygous115569732
71227535012275351CT26GENIChomozygous115569733
71227543212275433TC28GENIChomozygous115569734
71227561112275612TC11GENIChomozygous115569735
71227569712275698TC16GENIChomozygous115569736
71227570012275701TG16GENIChomozygous115569737
71227571012275711CG16GENIChomozygous115569738
71227584912275850T16GENICpossibly homozygous128435705
71227633412276335TC18GENIChomozygous115569739
71227774512277746GT23GENIChomozygous115569740
71227860512278606CT17GENIChomozygous115569741
71227878012278781TC18GENIChomozygous115569742
71227892512278926GA25GENIChomozygous115569743
71227925212279253AG39GENIChomozygous115569744
71228014812280149CA24GENIChomozygous115569745
71228027612280277CT26GENIChomozygous115569746
71227336512273366TG16GENIChomozygous118251029
71227713212277133CT16GENIChomozygous118251031