chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264094170264094171GT26GENIChomozygous987110135
1264094954264094955GA30GENIChomozygous987110136
1264095002264095003TC29GENIChomozygous987110137
1264095870264095871CT26GENIChomozygous987110138
1264095886264095887AG31GENIChomozygous987110139
1264096067264096068CG28GENIChomozygous987110140
1264096228264096229CA28GENIChomozygous987110141
1264096229264096230AT27GENIChomozygous987110142
1264096802264096803GA35GENIChomozygous987110143
1264096893264096894CA27GENIChomozygous987110144
1264096989264096990AG15GENIChomozygous987110145
1264097432264097433TC35GENIChomozygous987110146
1264097484264097485TC37GENIChomozygous987110147
1264097567264097568GA23GENIChomozygous987110148
1264097573264097574GC23GENIChomozygous987110149
1264097633264097634AC27GENIChomozygous987110150
1264097768264097769AG37GENIChomozygous987110151
1264097829264097830TC39GENIChomozygous987110152
1264097921264097922AC27GENIChomozygous987110153
1264097923264097924AT29GENIChomozygous987110154
1264098124264098125TC28GENIChomozygous987110155
1264098178264098179GA20GENIChomozygous987110156
1264098215264098216TC16GENIChomozygous987110157
1264099322264099323TC30GENIChomozygous987110158
1264099341264099342AG33GENIChomozygous987110159
1264099343264099344AC35GENIChomozygous987110160
1264099366264099367GA35GENIChomozygous987110161
1264099541264099542GA29GENIChomozygous987110162
1264100050264100051GC28GENIChomozygous987110163
1264100146264100147TC6GENIChomozygous987110164
1264100637264100638TC24GENIChomozygous987110165
1264100900264100901TG33GENIChomozygous987110166
1264103344264103345CT17GENIChomozygous987110167