chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56346370763463708CG18GENIChomozygous55423876
56346388263463883AC18GENICpossibly homozygous55423878
56346392163463922AG17GENIChomozygous55423880
56346405163464052GC29GENIChomozygous55423882
56346518263465183CT27GENIChomozygous55423886
56346520263465203CT30GENIChomozygous55423887
56346544163465442CG22GENIChomozygous55423889
56346547863465481CCT---20GENIChomozygous55423891
56346548463465486GA--17GENIChomozygous55423893
56346556063465561CA31GENIChomozygous55423895
56346556563465567TA--29GENIChomozygous55423897
56346558563465586TC29GENIChomozygous55423899
56346625863466259GA35GENIChomozygous55423901
56346629163466292GGC31GENIChomozygous55423903
56346642563466426CA27GENIChomozygous55423905
56346648863466489GA36GENIChomozygous55423907
56346651963466520GA36GENIChomozygous55423909
56346662363466624AG18GENIChomozygous55423911
56346668463466685GGA17GENIChomozygous55423913
56346668563466686CG16GENIChomozygous56347948
56346669363466694CT19GENIChomozygous55423917
56346672363466724GT22GENIChomozygous55423919
56346680363466804CT35GENIChomozygous55423921
56346691363466914AG24GENIChomozygous55423923
56346691463466915TG21GENIChomozygous55423925
56346694463466945TC30GENIChomozygous55423927
56346694663466947GA30GENIChomozygous55423929
56346711463467115TC27GENIChomozygous55423931
56346753563467536GA23GENIChomozygous55423933
56346754263467543GA22GENIChomozygous55423935
56346773163467732AG19GENIChomozygous55423937
56346779663467797CT29GENIChomozygous55423939
56346781463467815AG30GENIChomozygous55423941
56346855963468560TG18GENIChomozygous55423943
56346874563468746GC35GENIChomozygous55423945
56346927063469271GC31GENIChomozygous55423947