chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125310298253102983GA32GENICpossibly homozygous50255574
125310310053103101GA35GENICpossibly homozygous50255576
125310387853103879GA25GENIChomozygous50255578
125310428953104290CT23GENIChomozygous50255580
125310481153104812TC27GENIChomozygous50255582
125310534053105341TC31GENIChomozygous50255584
125310556353105564GGT28GENIChomozygous50255586
125310593553105936GA27GENIChomozygous50255588
125310616353106164TTTG22GENICpossibly homozygous50255590
125310629153106292GA21GENIChomozygous50255592
125310658853106589GA23GENIChomozygous50255594
125310695853106959CT16GENIChomozygous50255602
125310739953107400TA28GENIChomozygous50255604
125310759953107600TA17GENIChomozygous50255606
125310762453107625TTA18GENICpossibly homozygous50255608
125310774153107742CG24GENIChomozygous50255610
125310784253107843TC4GENICheterozygous50255612
125310851453108515TC11GENIChomozygous50255632
125310851753108518CCT9GENIChomozygous50255634