chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1281066400281066401GA12GENIChomozygous931275311
1281066783281066784CT11GENIChomozygous931275312
1281067900281067901GA8GENIChomozygous931275313
1281068938281068939AG8GENIChomozygous931275314
1281069137281069138TC8GENIChomozygous931275315
1281071635281071636CT8GENIChomozygous931275316
1281072910281072911CA14GENIChomozygous931275317
1281073051281073052AC12GENIChomozygous931275318
1281073112281073113CT15GENIChomozygous931275319
1281074099281074100TA11GENIChomozygous931275320
1281074239281074240AG14GENIChomozygous931275321
1281074948281074949TC11GENIChomozygous931275322
1281076716281076717TC11GENIChomozygous931275323
1281079975281079976CT15GENIChomozygous931275324
1281080337281080338TC10GENIChomozygous931275325
1281081528281081529TC5GENIChomozygous931275326
1281083336281083337GA6GENIChomozygous931275327
1281083372281083373CT8GENIChomozygous931275328
1281083424281083425CT7GENIChomozygous931275329
1281085991281085992TC16GENIChomozygous931275330
1281086118281086119TC10GENICpossibly homozygous931275331
1281086540281086541CT12GENIChomozygous931275332
1281086554281086555GT14GENIChomozygous931275333
1281087981281087982CA8GENIChomozygous931275334
1281088091281088092CA14GENIChomozygous931275335
1281088652281088653GA19GENIChomozygous931275336
1281088756281088757GA13GENIChomozygous931275337
1281090301281090302TC8GENIChomozygous931275338
1281090501281090502AG9GENIChomozygous931275339
1281092719281092720AG14GENIChomozygous931275340
1281094672281094673AG11GENIChomozygous931275341
1281095950281095951CA7GENIChomozygous931275342
1281097018281097019CA14GENIChomozygous931275343
1281097340281097341AT11GENIChomozygous931275344
1281097811281097812TG8GENIChomozygous931275345
1281100536281100537AT3GENIChomozygous931275346