chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150686278150686279CT12GENIChomozygous946983671
5150687272150687273CT19GENIChomozygous946983672
5150688837150688838TC17GENIChomozygous946983673
5150690664150690665GA23GENIChomozygous946983674
5150690906150690907TC26GENICpossibly homozygous946983675
5150691388150691389CT10GENIChomozygous946983676
5150691430150691431AG18GENIChomozygous946983677
5150692118150692119TA5GENIChomozygous946983678
5150692120150692121GC5GENIChomozygous946983679
5150692122150692123TC6GENIChomozygous946983680
5150692348150692349AG13GENIChomozygous946983681
5150694736150694737TC9GENIChomozygous946983682
5150695760150695761CT26GENIChomozygous946983683
5150696850150696851GA8GENIChomozygous946983684
5150697663150697664GA7GENIChomozygous946983685
5150699962150699963CT19GENIChomozygous946983686
5150700269150700270GA23GENIChomozygous946983687
5150701466150701467TC32GENIChomozygous946983688
5150702419150702420CT20GENIChomozygous946983689
5150703071150703072AC14GENIChomozygous946983690