chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157581407157581408CT57GENIChomozygous112906692
4157584722157584723TA24GENICpossibly homozygous112906696
4157586278157586279AG44GENIChomozygous112906698
4157586839157586840CT57GENIChomozygous112906700
4157587009157587010CA50GENIChomozygous112906702
4157587565157587566CT42GENIChomozygous112906704
4157587876157587877AC48GENIChomozygous112906706
4157588993157588994AT40GENICpossibly homozygous112906708
4157590274157590275TC32GENIChomozygous112906712
4157591508157591509GA38GENIChomozygous112906714
4157586817157586817A57GENIChomozygous128096207
4157589708157589708CTCTCTGTT17GENIChomozygous128096208
4157593016157593017AT31GENICpossibly homozygous113062915
4157593166157593167A38GENICpossibly homozygous128096209