chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125310298253102983GA14GENIChomozygous50255574
125310310053103101GA17GENIChomozygous50255576
125310387853103879GA22GENIChomozygous50255578
125310428953104290CT20GENICpossibly homozygous50255580
125310481153104812TC19GENICheterozygous50255582
125310534053105341TC4GENIChomozygous50255584
125310556353105564GGT7GENICpossibly homozygous50255586
125310593553105936GA3GENIChomozygous50255588
125310616353106164TTTG2GENIChomozygous50255590
125310629153106292GA20GENIChomozygous50255592
125310658853106589GA9GENIChomozygous50255594
125310695853106959CT1GENIChomozygous50255602
125310739953107400TA23GENICpossibly homozygous50255604
125310759953107600TA9GENICpossibly homozygous50255606
125310762453107625TTA1GENIChomozygous50255608
125310774153107742CG25GENIChomozygous50255610
125310851453108515TC2GENIChomozygous50255632
125310851753108518CCT2GENIChomozygous50255634