chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1281066324281066325TA3GENICheterozygous125330365
1281066400281066401GA16GENIChomozygous108669326
1281066783281066784CT15GENIChomozygous108669327
1281067900281067901GA9GENIChomozygous108669328
1281068938281068939AG6GENIChomozygous108669329
1281071635281071636CT10GENIChomozygous108669331
1281072910281072911CA27GENIChomozygous108669332
1281073051281073052AC13GENIChomozygous108669333
1281073112281073113CT16GENIChomozygous108669334
1281074099281074100TA17GENIChomozygous108669335
1281074239281074240AG23GENIChomozygous108669336
1281074948281074949TC9GENIChomozygous108669337
1281076716281076717TC19GENIChomozygous108669338
1281079975281079976CT16GENIChomozygous108669339
1281080337281080338TC13GENIChomozygous108669340
1281081528281081529TC18GENIChomozygous108669341
1281083336281083337GA14GENIChomozygous108669342
1281083372281083373CT14GENIChomozygous108669343
1281083424281083425CT11GENIChomozygous108669344
1281086118281086119TC15GENIChomozygous108669346
1281086540281086541CT9GENIChomozygous108669347
1281086554281086555GT14GENIChomozygous108669348
1281087981281087982CA18GENIChomozygous108669349
1281088091281088092CA4GENIChomozygous108669350
1281088652281088653GA16GENIChomozygous108669351
1281088756281088757GA22GENIChomozygous108669352
1281090301281090302TC18GENIChomozygous108669353
1281090501281090502AG12GENIChomozygous108669354
1281090603281090604GA8GENICheterozygous125330366
1281090631281090632CT8GENICheterozygous125330367
1281090655281090656AG6GENICheterozygous121236336
1281090710281090711GC13GENICheterozygous108669355
1281092719281092720AG18GENIChomozygous108669357
1281094672281094673AG5GENIChomozygous108669358
1281097018281097019CA16GENIChomozygous108669361
1281097340281097341AT13GENIChomozygous108669362
1281097811281097812TG13GENIChomozygous108669363