chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116371048116371049AC20GENIChomozygous116669113
8116373998116373999TC22GENIChomozygous116669115
8116374290116374291CT26GENIChomozygous116669117
8116374344116374345AC26GENIChomozygous116669119
8116374711116374712TC26GENIChomozygous116669121
8116374894116374895GA23GENIChomozygous116669123
8116374962116374963AG30GENIChomozygous116669125
8116374976116374977CG35GENIChomozygous116669127
8116377155116377156AC34GENIChomozygous116669139
8116377878116377879TA12GENIChomozygous116669141
8116378976116378977GA27GENIChomozygous116669145
8116379424116379425AC36GENIChomozygous116669147
8116379895116379896TA31GENIChomozygous116669149
8116380205116380206GT33GENIChomozygous116669151
8116380657116380658TC36GENIChomozygous116669153
8116380670116380671AG35GENIChomozygous116669155
8116380846116380847TC35GENIChomozygous116669157
8116380872116380873AG38GENIChomozygous117912549
8116380873116380874GA37GENIChomozygous116886429
8116380881116380882AG39GENIChomozygous116669159
8116381176116381177GA38GENIChomozygous116669161
8116381260116381261GA24GENIChomozygous116669163
8116381577116381578AG27GENIChomozygous116669165
8116381652116381653CT33GENIChomozygous116669167
8116381760116381761TC29GENIChomozygous116669169
8116382042116382043CT49GENIChomozygous116669173
8116382077116382078GA43GENIChomozygous116669175
8116383487116383488GA22GENIChomozygous116669177
8116384688116384689AG30GENIChomozygous116669183
8116384693116384694AT26GENIChomozygous116669185
8116384694116384695CG26GENIChomozygous116669187
8116385400116385401TC29GENIChomozygous116669189
8116386724116386725AG18GENIChomozygous116669191
8116386945116386946CG17GENIChomozygous116669193
8116386952116386953CT16GENIChomozygous116988053
8116387506116387507GA35GENIChomozygous116669195