chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57897621078976211CA22GENICpossibly homozygous113885238
57897676878976769TC21GENIChomozygous113885243
57897710478977105TC22GENIChomozygous113885245
57897724478977245GA22GENIChomozygous113885247
57897781178977812CA13GENIChomozygous119203609
57897843478978435CT16GENIChomozygous113885250
57897927578979276CT17GENIChomozygous113885252
57897982178979822TC17GENIChomozygous113885254
57897786778977868AC19GENIChomozygous119169785
57898044878980449CA15GENIChomozygous119169787
57898101978981020AG25GENICpossibly homozygous113885256
57898198878981989CA20GENIChomozygous113885258
57898200378982004TC18GENIChomozygous113885260
57898245778982458TC14GENIChomozygous113885262
57898346578983466TC8GENIChomozygous113885266
57898354078983541GA10GENIChomozygous119169789
57898438378984384CT25GENIChomozygous119169791
57898460878984609CT11GENIChomozygous114635289
57898038778980387T6GENIChomozygous131386317
57898108078981082GA17GENIChomozygous128201908