chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145471891145471892CT16GENIChomozygous119315545
4145472193145472194A20GENIChomozygous132967684
4145472230145472231CT16GENIChomozygous119315546
4145472369145472370TC24GENIChomozygous112870906
4145472937145472938A27GENIChomozygous128087995
4145474303145474304CT15GENICpossibly homozygous119442649
4145476320145476320G9GENIChomozygous132967685
4145476776145476777GT18GENIChomozygous113179002
4145477153145477154TC18GENIChomozygous113179003
4145477850145477851AG15GENIChomozygous113179005
4145480158145480159GA19GENIChomozygous119315547
4145480529145480530TC15GENIChomozygous112870909
4145481623145481624AG16GENIChomozygous119315548
4145481733145481734CT18GENIChomozygous112870910
4145481748145481749CG17GENIChomozygous112870911
4145482380145482381TA11GENIChomozygous119315549
4145482848145482849CT16GENIChomozygous119315550
4145483299145483299AT15GENICpossibly homozygous132967686
4145485492145485493TC14GENIChomozygous119315551
4145485656145485657CT20GENIChomozygous112870914
4145485793145485794GT18GENIChomozygous112870915
4145486088145486089CG23GENIChomozygous113179008
4145486325145486326GT28GENIChomozygous112870917
4145486784145486785GC25GENIChomozygous112870918