chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34632746746327468GA27GENIChomozygous774673055
34632800646328007AG18GENIChomozygous774673056
34632844746328448CA28GENIChomozygous774673057
34632878946328790CT16GENIChomozygous774673058
34632894746328948CT22GENIChomozygous774673059
34632896346328964AG22GENIChomozygous774673060
34632946946329470GT46GENIChomozygous774673061
34633021546330216TA39GENIChomozygous774673062
34633045446330455GA31GENIChomozygous774673063
34633095346330954GA25GENIChomozygous774673064
34633115346331154AG23GENIChomozygous774673065
34633631246336313TC61GENIChomozygous774673066
34633638346336384TG52GENIChomozygous774673067
34633742646337427AC35GENICpossibly homozygous774673068
34633904246339043AG48GENIChomozygous774673069
34633938046339381TC37GENIChomozygous774673070
34634092946340930CT58GENIChomozygous774673071
34634136046341361CT44GENIChomozygous774673072
34634192146341922AG24GENIChomozygous774673073
34634200946342010GT40GENIChomozygous774673074
34634218446342185TC27GENIChomozygous774673075
34634448746344488AT31GENIChomozygous774673076
34634632146346322CT41GENIChomozygous774673077
34634656446346565AG29GENIChomozygous774673078
34634845946348460TC14GENICpossibly homozygous774673079
34634973746349738AG43GENIChomozygous774673080
34634998246349983TA29GENIChomozygous774673081
34635100646351007AG30GENIChomozygous774673082
34635180346351804TC27GENIChomozygous774673083
34635198746351988CG18GENIChomozygous774673084
34635198846351989AT19GENIChomozygous774673085
34635206546352066AC34GENICheterozygous774673086
34635207146352072TC38GENICheterozygous774673087
34635456446354565TA32GENIChomozygous774673088
34635791146357912GA34GENIChomozygous774673089
34635826746358268CT29GENIChomozygous774673090