chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4123120706123120707CG43GENIChomozygous113155722
4123120737123120738CT50GENIChomozygous113155724
4123121721123121722GC18GENICheterozygous119464550
4123122253123122254GA30GENIChomozygous113155725
4123122695123122696AG56GENIChomozygous113155726
4123122898123122899TC56GENIChomozygous113155727
4123123210123123211CT44GENIChomozygous113155728
4123123615123123616GA35GENIChomozygous113155729
4123123662123123663GA38GENIChomozygous113155730
4123124319123124320GA42GENIChomozygous113155731
4123124424123124425GA36GENIChomozygous113155732
4123125117123125118AC39GENIChomozygous113155733
4123125603123125604AG18GENIChomozygous113155734
4123127367123127368AG42GENIChomozygous113155735
4123127975123127976GT23GENICpossibly homozygous113049332
4123128272123128273GA45GENIChomozygous113155736
4123130582123130583GA41GENICpossibly homozygous113155737
4123131458123131459CT36GENIChomozygous113155738
4123132304123132305CT39GENIChomozygous113155739