chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118133268881332689AAC15GENICpossibly homozygous50843773
118133279581332796TC18GENICpossibly homozygous50843774
118133359481333595TC27GENIChomozygous50843780
118133527781335278CA31GENICpossibly homozygous51238292
118133641781336418TC9GENICheterozygous50843800
118133738081337381A-7GENICheterozygous51170658
118133776581337766CT27GENIChomozygous51238294
118133899481338995GGC19GENICpossibly homozygous51238296
118133899581338996C-19GENICheterozygous50843817
118133933381339334GA25GENIChomozygous51238297
118134096681340967CT16GENIChomozygous51146971
118134126581341266CT12GENIChomozygous51238299
118134184481341845AG14GENICpossibly homozygous50843825
118134190281341903AG15GENICheterozygous50843826
118134271381342714CT16GENIChomozygous50843827
118134281781342818AC23GENIChomozygous51238300
118134298581342986TA18GENIChomozygous51238301
118134370581343706TC34GENICpossibly homozygous50843829
118134379981343800TC27GENIChomozygous51051227
118134397081343971AG25GENICpossibly homozygous51051228
118134401081344011AG14GENIChomozygous51238303
118134406481344065TA28GENICpossibly homozygous50843830
118134432681344327TA28GENIChomozygous51022804