chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
43475733134757332TC18GENIChomozygous895582722
43475806834758069TC12GENIChomozygous895582723
43475828734758288TC9GENIChomozygous895582724
43475856634758567TC22GENIChomozygous895582725
43475938834759389GA12GENIChomozygous895582726
43475972534759726GT17GENIChomozygous895582727
43476055034760551AG24GENICpossibly homozygous895582728
43476057034760571CT23GENIChomozygous895582729
43476095334760954GA9GENIChomozygous895582730
43476095834760959CA7GENIChomozygous895582731
43476098634760987CT11GENIChomozygous895582732
43476139634761397AG13GENIChomozygous895582733
43476156334761564GT12GENIChomozygous895582734
43476268734762688CT15GENIChomozygous895582735
43476301734763018GA10GENIChomozygous895582736
43476316434763165TC14GENIChomozygous895582737
43476381434763815AG17GENIChomozygous895582738
43476428434764285GA13GENIChomozygous895582739
43476448134764482TC17GENIChomozygous895582740