chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5161451441161451442GA51GENIChomozygous141770590
5161451455161451456GA54GENIChomozygous141770591
5161452091161452092CT18GENIChomozygous141770592
5161452744161452745CG40GENIChomozygous137661724
5161453002161453003CT42GENICpossibly homozygous137661725
5161453098161453099TG44GENICpossibly homozygous137661726
5161453546161453547GC46GENICpossibly homozygous137661727
5161453743161453744TG47GENIChomozygous137661728
5161453890161453891CT43GENICpossibly homozygous141770593
5161454013161454013T45GENIChomozygous137351855
5161454557161454558GA55GENICpossibly homozygous141770594
5161454827161454828TC65GENIChomozygous137661729
5161454890161454891TG48GENIChomozygous137661731
5161455018161455019TC47GENIChomozygous137661732
5161455383161455384GA48GENIChomozygous141770595
5161455430161455431TC46GENIChomozygous137661733
5161455848161455849CT44GENIChomozygous141770596
5161452441161452442CT27GENICpossibly homozygous144363606