chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145440759145440760AT31GENIChomozygous119315523
4145441975145441976CT28GENIChomozygous119315524
4145442116145442117AG16GENIChomozygous119315525
4145442170145442171AG28GENIChomozygous112870891
4145443014145443015TA18GENIChomozygous112870892
4145443074145443075AG20GENIChomozygous119315526
4145443138145443139AG24GENIChomozygous119315527
4145443549145443550TC24GENIChomozygous112870893
4145443680145443681AG13GENICpossibly homozygous119315528
4145443974145443975AG26GENIChomozygous112870894
4145444031145444032TC26GENIChomozygous119315529
4145444815145444816AG24GENIChomozygous119315530
4145448310145448311CA28GENIChomozygous112870896
4145448855145448856CA27GENIChomozygous119315531
4145449731145449732AG24GENIChomozygous119315532
4145449876145449877GA22GENIChomozygous119315533
4145442882145442883T25GENIChomozygous132967676
4145443287145443288A16GENIChomozygous132967677
4145443713145443713A31GENIChomozygous132967678
4145447736145447737AT21GENIChomozygous132973207
4145447738145447739TA21GENIChomozygous132973208
4145447773145447777CACA24GENIChomozygous132967680
4145447767145447769AA23GENIChomozygous132967679