chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108703544487035445CT14GENIChomozygous53161830
108703549587035496GC17GENIChomozygous51725050
108703589387035894CG15GENIChomozygous52848380
108703593987035940GA14GENIChomozygous51529694
108703639587036396TA13GENIChomozygous51529696
108703644687036447CT12GENIChomozygous51529697
108703676387036764GA29GENIChomozygous51529706
108703677287036773AG28GENIChomozygous53161832
108703683987036840CT16GENIChomozygous53544777
108703690687036907GC14GENIChomozygous53161834
108703929187039292TC8GENIChomozygous51529735
108704066487040665TG13GENIChomozygous51529736
108704079787040798AT22GENIChomozygous53161839
108704114087041141TC14GENIChomozygous51529737
108704114687041147TC14GENIChomozygous51529738
108704115287041153CT12GENIChomozygous53161841
108704149687041497AG7GENIChomozygous51529739
108704165487041658CCCC----7GENIChomozygous51529742
108704182687041827C-9GENIChomozygous53161843
108704220087042201AG7GENIChomozygous53161845
108704229187042292AG9GENIChomozygous53161847
108704239387042394AG9GENIChomozygous53161849
108704274187042742TC9GENIChomozygous51529744
108704282387042824GA13GENIChomozygous53161851
108704287087042871G-8GENIChomozygous53161853
108704287887042879GA9GENIChomozygous53161855
108704302587043026AG14GENIChomozygous53161857
108704337687043377TC11GENIChomozygous51529748
108704352487043525GA9GENIChomozygous53161859
108704373687043737TC8GENIChomozygous51529752