chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4150316167150316168GA30GENIChomozygous57953034
4150316684150316685CA39GENICpossibly homozygous57953037
4150316694150316695TC38GENIChomozygous56980684
4150316858150316859CG31GENIChomozygous56980685
4150317245150317246AT30GENIChomozygous56980686
4150317300150317301A-34GENIChomozygous58157026
4150317744150317745TA35GENIChomozygous56980687
4150317901150317902CT17GENIChomozygous58157028
4150318030150318031CT26GENIChomozygous58157030
4150318787150318788TA43GENIChomozygous57953040
4150318823150318824TC47GENIChomozygous56980689
4150318909150318910GA49GENIChomozygous58157032
4150319228150319229TC28GENIChomozygous57953043