chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5131841339131841340AG58GENIChomozygous775427632
5131842186131842187AC41GENIChomozygous775427633
5131842813131842814GA22GENIChomozygous775427634
5131844777131844778GA54GENIChomozygous775427635
5131845402131845403CT54GENIChomozygous775427636
5131845727131845728CA40GENIChomozygous775427637
5131846180131846181TG32GENIChomozygous775427638
5131848908131848909TG59GENIChomozygous775427639
5131849533131849534AG59GENICheterozygous775427640
5131849561131849562TG66GENICheterozygous775427641
5131849567131849568CT66GENICheterozygous775427642
5131849596131849597CA63GENICheterozygous775427643
5131849599131849600GA64GENICheterozygous775427644
5131849639131849640CA60GENICheterozygous775427645
5131849643131849644TC63GENICheterozygous775427646
5131849650131849651AC62GENICheterozygous775427647
5131849672131849673CT47GENICpossibly homozygous775427648
5131850089131850090AT22GENIChomozygous775427649
5131852932131852933CA33GENIChomozygous775427650
5131853410131853411AG47GENIChomozygous775427651
5131853511131853512TG64GENIChomozygous775427652
5131853678131853679TC40GENIChomozygous775427653
5131854297131854298CA47GENIChomozygous775427654
5131855380131855381CG56GENIChomozygous775427655
5131859483131859484TC48GENIChomozygous775427656
5131859936131859937GA55GENIChomozygous775427657
5131861443131861444GT47GENICpossibly homozygous775427658
5131862290131862291CG51GENICpossibly homozygous775427659
5131864052131864053CT24GENIChomozygous775427660