chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41096893510968936CT9GENIChomozygous57801470
41096896410968965TC9GENIChomozygous56747667
41096908110969082CCTTT4GENICheterozygous56747668
41096908110969082CCTTTT4GENICheterozygous58327248
41096921010969211GA11GENIChomozygous56747669
41096944810969449CT9GENIChomozygous57801473
41096955710969558CCT10GENIChomozygous56747670
41097053110970532TC16GENIChomozygous56747672
41097064910970650CA17GENIChomozygous57801475
41097068110970682AC19GENIChomozygous57801477
41097078810970789GA23GENIChomozygous56747673
41097080210970803AC26GENIChomozygous56747674
41097104010971046CAACAC------15GENIChomozygous56747675
41097104610971047CG13GENIChomozygous58327249
41097105310971054AG15GENIChomozygous56747678
41097104910971050CG15GENIChomozygous56747676
41097105010971051TTG15GENIChomozygous56747677
41097105110971052CA15GENIChomozygous58327250
41097135010971351GA17GENIChomozygous56747679
41097154410971545AG18GENIChomozygous56747680
41097212510972126GC2GENIChomozygous56747684
41097227310972274CCCCTG6GENIChomozygous57801480
41097361010973611CG11GENIChomozygous58584431
41097361210973613TC10GENIChomozygous56747689
41097461010974611TG17GENIChomozygous56747694
41097491910974920CA25GENIChomozygous56747695
41097528410975285AG28GENIChomozygous56747697
41097583210975833CCTT21GENIChomozygous57801482
41097606910976070CT12GENIChomozygous57801484
41097634410976345GA32GENIChomozygous57801487
41097675410976755CT35GENIChomozygous57801489
41097724910977250TC15GENIChomozygous56747715
41097803810978039GA21GENIChomozygous57801491
41097837910978380GGAGAGCTGTAACACTAAGA14GENICpossibly homozygous58327252
41097855510978556TTACACACACAC3GENIChomozygous58327253
41097893310978934G-27GENIChomozygous57801493
41097964210979643AG33GENIChomozygous57801496
41097969810979699GGGCCTTTGCCTAAAGACAAATGGTTT18GENIChomozygous58584433
41097996610979967AC39GENIChomozygous56747723
41098039810980399TC26GENIChomozygous56747724
41098079110980792CT22GENIChomozygous57801498