chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264095442264095443AG29GENIChomozygous948974127
1264095886264095887AG25GENIChomozygous948974128
1264097432264097433TC17GENIChomozygous948974129
1264097633264097634AC20GENIChomozygous948974130
1264097682264097683GA20GENIChomozygous948974131
1264099882264099883CT9GENIChomozygous948974132
1264099931264099932CT8GENIChomozygous948974133
1264100059264100060TA16GENIChomozygous948974134
1264100188264100189AG16GENIChomozygous948974135
1264100432264100433GA15GENIChomozygous948974136
1264100637264100638TC18GENIChomozygous948974137
1264100851264100852AG23GENIChomozygous948974138
1264100853264100854AT23GENIChomozygous948974139
1264101725264101726TA12GENIChomozygous948974140
1264101841264101842AG12GENIChomozygous948974141
1264102013264102014GA16GENIChomozygous948974142
1264102022264102023CT18GENIChomozygous948974143
1264102091264102092GA7GENIChomozygous948974144
1264102112264102113TC9GENIChomozygous948974145
1264102373264102374GA22GENIChomozygous948974146
1264102418264102419TC19GENIChomozygous948974147
1264102632264102633CT22GENIChomozygous948974148
1264103104264103105GA15GENIChomozygous948974149
1264103285264103286AG23GENIChomozygous948974150
1264103682264103683CT16GENIChomozygous948974151
1264104414264104415GA17GENIChomozygous948974152