chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45805351358053514TA24GENIChomozygous112660148
45805509458055095CG29GENIChomozygous112660152
45805571258055713GT16GENIChomozygous119276897
45805571358055714TG16GENIChomozygous113274229
45805577758055778CT12GENIChomozygous119276899
45805577858055779TC12GENIChomozygous119276901
45805584458055845GC18GENIChomozygous112660155
45805628358056284TA18GENIChomozygous119276903
45805628458056285CT17GENIChomozygous119276905
45805644158056442TA17GENIChomozygous119338192
45805660558056606TA13GENIChomozygous119276907
45805660658056607AG12GENIChomozygous119276909
45805671758056718GA16GENIChomozygous119276911
45805671858056719TG16GENIChomozygous119276913
45805675658056757CG13GENIChomozygous119453922
45805677858056779TG9GENIChomozygous119369828
45805680058056801CG6GENIChomozygous119498475
45805680158056802GC6GENIChomozygous119276915
45805687958056880GA13GENIChomozygous112660161
45805693158056932TA14GENIChomozygous112660163
45805694958056950TG13GENIChomozygous119276917
45805704758057048GT21GENIChomozygous119276919
45805888358058884GA25GENIChomozygous112660165
45805952958059530GA27GENIChomozygous112660167
45805993158059932GT20GENIChomozygous112660171
45805993758059938CT21GENIChomozygous112660173
45806024558060246TA19GENIChomozygous112660175
45806049358060494AG22GENIChomozygous112660177
45806064858060649CA16GENIChomozygous112660179
45806112358061124GA21GENIChomozygous112660181
45806173058061731TC26GENIChomozygous112660183