chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125310298253102983GA25GENIChomozygous50255574
125310310053103101GA29GENICpossibly homozygous50255576
125310387853103879GA18GENIChomozygous50255578
125310428953104290CT32GENIChomozygous50255580
125310481153104812TC26GENIChomozygous50255582
125310534053105341TC28GENIChomozygous50255584
125310556353105564GGT28GENIChomozygous50255586
125310593553105936GA19GENIChomozygous50255588
125310616353106164TTTG20GENIChomozygous50255590
125310629153106292GA28GENIChomozygous50255592
125310658853106589GA26GENIChomozygous50255594
125310695853106959CT27GENIChomozygous50255602
125310739953107400TA33GENIChomozygous50255604
125310759953107600TA15GENIChomozygous50255606
125310762453107625TTA15GENICpossibly homozygous50255608
125310774153107742CG20GENIChomozygous50255610
125310784253107843TC16GENIChomozygous50255612
125310851453108515TC28GENIChomozygous50255632
125310851753108518CCT28GENIChomozygous50255634