chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1281066783281066784CT26GENIChomozygous108669327
1281067900281067901GA22GENIChomozygous108669328
1281068938281068939AG21GENIChomozygous108669329
1281069137281069138TC11GENIChomozygous108669330
1281071635281071636CT18GENIChomozygous108669331
1281072910281072911CA32GENICpossibly homozygous108669332
1281073051281073052AC25GENIChomozygous108669333
1281073112281073113CT33GENIChomozygous108669334
1281074099281074100TA33GENIChomozygous108669335
1281074239281074240AG39GENIChomozygous108669336
1281074948281074949TC19GENIChomozygous108669337
1281076716281076717TC18GENIChomozygous108669338
1281079975281079976CT11GENIChomozygous108669339
1281080337281080338TC26GENIChomozygous108669340
1281081528281081529TC18GENIChomozygous108669341
1281083336281083337GA16GENIChomozygous108669342
1281083372281083373CT16GENICpossibly homozygous108669343
1281083424281083425CT16GENICpossibly homozygous108669344
1281085991281085992TC14GENIChomozygous108669345
1281086118281086119TC42GENIChomozygous108669346
1281086540281086541CT21GENIChomozygous108669347
1281086554281086555GT22GENIChomozygous108669348
1281087981281087982CA24GENIChomozygous108669349
1281088091281088092CA35GENIChomozygous108669350
1281088652281088653GA29GENIChomozygous108669351
1281088756281088757GA42GENIChomozygous108669352
1281090301281090302TC27GENIChomozygous108669353
1281090501281090502AG24GENIChomozygous108669354
1281092719281092720AG25GENIChomozygous108669357
1281094672281094673AG38GENIChomozygous108669358
1281095916281095917AG24GENIChomozygous108669359
1281095950281095951CA27GENIChomozygous108669360
1281097018281097019CA28GENIChomozygous108669361
1281097340281097341AT28GENIChomozygous108669362
1281097811281097812TG21GENIChomozygous108669363
1281100536281100537AT6GENIChomozygous108669364