chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2040229044022905CT41GENIChomozygous63640923
2040231234023124CT17GENICpossibly homozygous63640924
2040231544023155AG10GENICpossibly homozygous63335515
2040232834023284TC23GENIChomozygous63335516
2040234294023430GA25GENIChomozygous63335517
2040237874023788CT35GENIChomozygous63335518
2040239644023965GA18GENIChomozygous63335519
2040242264024227CT5GENIChomozygous63640925
2040252374025238AG15GENIChomozygous63335520
2040254904025491GA30GENIChomozygous63335521
2040256344025635CT18GENIChomozygous63335522
2040271444027145CT38GENIChomozygous63640928
2040275984027599GA22GENIChomozygous63335523
2040279374027938TC17GENIChomozygous63335524
2040281264028127AT23GENIChomozygous63335527
2040283234028324CT16GENIChomozygous63335528
2040289574028958GA28GENIChomozygous63640929
2040291844029185CG33GENICpossibly homozygous63640930
2040294634029464GA18GENIChomozygous63335529
2040299814029982GA30GENIChomozygous63640931
2040310994031100CA29GENIChomozygous63335530
2040314014031402AG38GENIChomozygous63640932
2040314044031405GA37GENIChomozygous63335532
2040316134031614GA20GENIChomozygous63640933
2040316664031667CT26GENIChomozygous63335533
2040317054031706CA25GENIChomozygous63335534
2040317524031753AT19GENIChomozygous63640934
2040318314031832CT23GENIChomozygous63335535
2040320374032038GA30GENIChomozygous63335537
2040328724032873GA20GENIChomozygous63640935
2040332264033227GA25GENICpossibly homozygous63640936