chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107136609771366098GA25GENIChomozygous116630172
107136619171366192AC26GENIChomozygous116630174
107136642971366430GA24GENIChomozygous116630176
107136706271367063TC24GENIChomozygous116630178
107136716171367162TC22GENIChomozygous116630180
107136779571367796TA18GENIChomozygous117223122
107136959071369591AG28GENIChomozygous116630184
107137327471373275GA30GENIChomozygous117223124
107137412371374124GC22GENIChomozygous116630186
107137504371375044GA29GENICpossibly homozygous117223126
107137520971375210GT32GENIChomozygous116630188
107137614571376146CT34GENIChomozygous116630192
107138193471381935TC28GENIChomozygous116630194