chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76794157667941576A20GENICpossibly homozygous144368132
76794317267943173CG17GENIChomozygous144374954
76794371567943715C11GENICpossibly homozygous144368133
76794454967944550GT24GENIChomozygous144374955
76794670467946706GA11GENIChomozygous144368134
76794672867946728C9GENICheterozygous144368135
76794700767947008GA20GENICpossibly homozygous144374956
76794788367947884GA31GENIChomozygous144374957
76794898767948988GT22GENIChomozygous144374958
76794941267949413TA39GENIChomozygous144374959
76794958267949583C25GENIChomozygous144368136
76795346667953467AG31GENIChomozygous144374960
76795449567954496G35GENIChomozygous144368137
76795470967954710GC27GENIChomozygous144374961
76795578567955785T22GENIChomozygous144368138
76795579567955796AT23GENIChomozygous144374962
76795663267956633GA40GENIChomozygous144374963
76795733767957338CG26GENIChomozygous144374964
76795738967957390CG26GENIChomozygous144374965
76795740467957405CT25GENIChomozygous144374966
76795831367958316CTC33GENIChomozygous144368139
76795959767959598AC38GENIChomozygous144374967
76796056667960567A35GENIChomozygous144368140
76796065067960650T27GENIChomozygous144368141
76796073767960738GA34GENIChomozygous144374968
76796276667962767C32GENIChomozygous144368142
76795347667953477TA35GENIChomozygous138112739
76795305767953058AT5GENIChomozygous149228335