chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18401931484019315CT30GENIChomozygous108879875
18401957784019578GA38GENICpossibly homozygous108879876
18401976284019763AC26GENIChomozygous109305069
18402025784020258CT26GENIChomozygous109305071
18402123984021240TC4GENIChomozygous108879881
18402124784021248TC3GENIChomozygous109305073
18402133584021336TC10GENIChomozygous108879882
18402138284021383TC12GENIChomozygous109305075
18402142784021428AG12GENICheterozygous108879883
18402142884021429TC12GENICheterozygous108879884
18402153884021539AG25GENIChomozygous108879885
18402208984022090CT27GENIChomozygous109305077
18402217884022179AT22GENIChomozygous108879886
18402218084022181GA23GENIChomozygous108879887
18402251184022512GA29GENIChomozygous108879888
18402297484022975TC14GENIChomozygous109305079
18402329084023291GA30GENIChomozygous109305081
18402423384024234AC26GENIChomozygous108879891
18402625584026256TC18GENIChomozygous108879893
18402656684026567AG30GENIChomozygous108879894
18402661284026613GA26GENIChomozygous109305083
18402676284026763CA14GENIChomozygous108879895
18402709384027094AG26GENIChomozygous108879896
18402815084028151TA20GENIChomozygous108879898
18402901084029011CT35GENIChomozygous109305085
18403111584031116AG36GENIChomozygous108879900
18403113084031131TG37GENIChomozygous108879901
18403243384032434GA38GENIChomozygous109305087
18403315884033159CT36GENIChomozygous109305089
18403369984033700CT43GENICpossibly homozygous109305091
18403648784036488TG29GENIChomozygous108879909
18403823084038231AT15GENIChomozygous108879912
18403931584039316CA20GENIChomozygous109305095
18403994284039943GT22GENIChomozygous109305097