chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----13GENIChomozygous711922879
3154514276154514277TG17GENIChomozygous569347743
3154514414154514415AAGTCT13GENIChomozygous711922881
3154514475154514476TC18GENIChomozygous569347744
3154514477154514478TC19GENIChomozygous569347745
3154515475154515476GA22GENIChomozygous569347746
3154515681154515682TA8GENIChomozygous569347747
3154516008154516009GA19GENIChomozygous569347748
3154516009154516010AT19GENIChomozygous569347749
3154516260154516261TC13GENIChomozygous569347750
3154516884154516885AG28GENIChomozygous569347751
3154517077154517078TC27GENIChomozygous571347786
3154517156154517157AG23GENIChomozygous569347752
3154517593154517594TC23GENIChomozygous569347753
3154517632154517633G-18GENIChomozygous711922882
3154517898154517899TC11GENIChomozygous569347754
3154517982154517986GGCA----18GENIChomozygous711922883
3154518068154518069GA17GENIChomozygous569347755
3154518158154518159TTA22GENIChomozygous711922884
3154518562154518563CT14GENIChomozygous571347787
3154518737154518738AG19GENIChomozygous569347756
3154518931154518932GGT11GENICheterozygous711922885
3154519100154519101CT7GENIChomozygous571347788
3154519184154519185CCA4GENIChomozygous711922886
3154519315154519316CT12GENIChomozygous569347757
3154519896154519897CCTT17GENICpossibly homozygous711922889
3154519985154519986AG19GENIChomozygous569347758
3154520058154520059TC18GENIChomozygous569347759
3154520781154520782TC22GENIChomozygous569347760
3154520987154520988CT16GENIChomozygous569347761
3154521914154521915TTAA12GENICpossibly homozygous711922891
3154521930154521931AAC10GENICheterozygous711922892
3154522134154522135AG18GENIChomozygous569347762