chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76794157667941576A27GENICpossibly homozygous144368132
76794317267943173CG26GENIChomozygous144374954
76794371567943715C15GENICpossibly homozygous144368133
76794454967944550GT27GENIChomozygous144374955
76794670467946706GA7GENIChomozygous144368134
76794672867946728C8GENICpossibly homozygous144368135
76794700767947008GA14GENIChomozygous144374956
76794788367947884GA24GENIChomozygous144374957
76794898767948988GT16GENIChomozygous144374958
76794941267949413TA24GENIChomozygous144374959
76794958267949583C20GENIChomozygous144368136
76795346667953467AG20GENICpossibly homozygous144374960
76795347667953477TA19GENICpossibly homozygous138112739
76795449567954496G22GENIChomozygous144368137
76795470967954710GC24GENIChomozygous144374961
76795578567955785T12GENIChomozygous144368138
76795579567955796AT13GENIChomozygous144374962
76795663267956633GA25GENIChomozygous144374963
76795733767957338CG26GENIChomozygous144374964
76795738967957390CG21GENIChomozygous144374965
76795740467957405CT19GENIChomozygous144374966
76795831367958316CTC21GENIChomozygous144368139
76795959767959598AC21GENIChomozygous144374967
76796056667960567A22GENIChomozygous144368140
76796065067960650T22GENIChomozygous144368141
76796073767960738GA16GENIChomozygous144374968
76796276667962767C4GENIChomozygous144368142
76795579567955796A13GENICheterozygous403895784