chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125310298253102983GA26GENIChomozygous50255574
125310310053103101GA19GENICpossibly homozygous50255576
125310387853103879GA15GENIChomozygous50255578
125310428953104290CT25GENIChomozygous50255580
125310481153104812TC36GENIChomozygous50255582
125310534053105341TC26GENIChomozygous50255584
125310556353105564GGT27GENIChomozygous50255586
125310593553105936GA30GENIChomozygous50255588
125310616353106164TTTG18GENICpossibly homozygous50255590
125310629153106292GA15GENIChomozygous50255592
125310658853106589GA30GENIChomozygous50255594
125310695853106959CT18GENIChomozygous50255602
125310739953107400TA27GENIChomozygous50255604
125310759953107600TA21GENIChomozygous50255606
125310762453107625TTA18GENICpossibly homozygous50255608
125310774153107742CG36GENIChomozygous50255610
125310784253107843TC2GENIChomozygous50255612
125310851453108515TC23GENIChomozygous50255632
125310851753108518CCT24GENIChomozygous50255634