chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18401931484019315CT16GENIChomozygous108879875
18401957784019578GA19GENIChomozygous108879876
18401976284019763AC18GENIChomozygous109305069
18402025784020258CT15GENIChomozygous109305071
18402153884021539AG8GENIChomozygous108879885
18402217884022179AT7GENIChomozygous108879886
18402218084022181GA7GENIChomozygous108879887
18402329084023291GA22GENIChomozygous109305081
18402423384024234AC16GENIChomozygous108879891
18402625584026256TC5GENIChomozygous108879893
18402656684026567AG11GENIChomozygous108879894
18402661284026613GA11GENIChomozygous109305083
18402709384027094AG10GENIChomozygous108879896
18402815084028151TA18GENIChomozygous108879898
18402901084029011CT11GENIChomozygous109305085
18403111584031116AG15GENIChomozygous108879900
18403113084031131TG16GENIChomozygous108879901
18403243384032434GA10GENIChomozygous109305087
18403315884033159CT19GENIChomozygous109305089
18403648784036488TG6GENIChomozygous108879909
18403823084038231AT22GENIChomozygous108879912
18403931584039316CA4GENIChomozygous109305095
18403994284039943GT17GENIChomozygous109305097