chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117255591117255592GA30GENICpossibly homozygous954829690
4117257889117257890CA36GENIChomozygous954829691
4117264298117264299GA43GENIChomozygous954829692
4117264605117264606AT27GENIChomozygous954829693
4117264644117264645CG20GENIChomozygous954829694
4117265590117265591CA45GENIChomozygous954829695
4117266654117266655AG26GENIChomozygous954829696
4117266678117266679GA26GENIChomozygous954829697
4117271434117271435TC23GENIChomozygous954829698
4117272285117272286AG9GENIChomozygous954829699
4117274282117274283TG25GENIChomozygous954829700
4117275127117275128AC16GENIChomozygous954829701
4117276347117276348CA14GENIChomozygous954829702
4117278270117278271GA25GENIChomozygous954829703
4117279197117279198TC17GENIChomozygous954829704
4117279408117279409TC31GENIChomozygous954829705
4117279581117279582GA28GENIChomozygous954829706
4117279704117279705TC24GENIChomozygous954829707
4117279791117279792AG35GENIChomozygous954829708
4117280030117280031AG51GENIChomozygous954829709
4117280142117280143GA43GENIChomozygous954829710
4117280653117280654CG14GENIChomozygous954829711
4117281056117281057GA28GENIChomozygous954829712
4117281183117281184GT30GENIChomozygous954829713
4117281563117281564CT27GENIChomozygous954829714
4117281635117281636GT30GENIChomozygous954829715
4117282050117282051TG28GENICpossibly homozygous954829716
4117282268117282269AG31GENIChomozygous954829717
4117282481117282482AC35GENIChomozygous954829718
4117282635117282636TC31GENIChomozygous954829719
4117283800117283801CT34GENIChomozygous954829720
4117284157117284158TC12GENIChomozygous954829721