chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107136580971365810GA22GENIChomozygous116630170
107136609771366098GA23GENIChomozygous116630172
107136619171366192AC18GENIChomozygous116630174
107136642971366430GA16GENIChomozygous116630176
107136706271367063TC15GENIChomozygous116630178
107136716171367162TC19GENIChomozygous116630180
107136760971367610AG12GENIChomozygous116630182
107136959071369591AG16GENIChomozygous116630184
107137412371374124GC17GENIChomozygous116630186
107137520971375210GT39GENIChomozygous116630188
107137613371376134CA13GENIChomozygous116630190
107137614571376146CT15GENIChomozygous116630192
107137884571378846AG19GENIChomozygous118000756
107138193471381935TC18GENIChomozygous116630194
107138217471382175TC22GENIChomozygous116630196