chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1281066400281066401GA57GENIChomozygous108669326
1281066783281066784CT57GENIChomozygous108669327
1281067900281067901GA34GENIChomozygous108669328
1281068938281068939AG32GENIChomozygous108669329
1281069137281069138TC20GENIChomozygous108669330
1281071635281071636CT39GENIChomozygous108669331
1281072910281072911CA45GENICpossibly homozygous108669332
1281073051281073052AC32GENICpossibly homozygous108669333
1281073112281073113CT34GENIChomozygous108669334
1281074099281074100TA50GENIChomozygous108669335
1281074239281074240AG49GENIChomozygous108669336
1281074948281074949TC70GENIChomozygous108669337
1281076716281076717TC46GENIChomozygous108669338
1281079975281079976CT55GENICpossibly homozygous108669339
1281080337281080338TC40GENIChomozygous108669340
1281081528281081529TC61GENIChomozygous108669341
1281083336281083337GA49GENIChomozygous108669342
1281083372281083373CT52GENIChomozygous108669343
1281083424281083425CT52GENIChomozygous108669344
1281084483281084484TA47GENICheterozygous109035506
1281085991281085992TC44GENIChomozygous108669345
1281086118281086119TC67GENIChomozygous108669346
1281086540281086541CT48GENIChomozygous108669347
1281086554281086555GT46GENIChomozygous108669348
1281087981281087982CA56GENIChomozygous108669349
1281088091281088092CA43GENIChomozygous108669350
1281088652281088653GA65GENIChomozygous108669351
1281088756281088757GA55GENIChomozygous108669352
1281090301281090302TC78GENIChomozygous108669353
1281090501281090502AG39GENIChomozygous108669354
1281090710281090711GC70GENICheterozygous108669355
1281090727281090728CT76GENICheterozygous108669356
1281092719281092720AG53GENIChomozygous108669357
1281094672281094673AG35GENIChomozygous108669358
1281095916281095917AG35GENIChomozygous108669359
1281095950281095951CA19GENIChomozygous108669360
1281097018281097019CA50GENIChomozygous108669361
1281097340281097341AT47GENIChomozygous108669362
1281097811281097812TG45GENIChomozygous108669363
1281100536281100537AT23GENIChomozygous108669364