chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----19GENIChomozygous725526779
3154514276154514277TG20GENIChomozygous592443183
3154514414154514415AAGTCT15GENIChomozygous725526781
3154514475154514476TC26GENIChomozygous592443184
3154514477154514478TC26GENIChomozygous592443185
3154515475154515476GA18GENIChomozygous592443186
3154515681154515682TA18GENIChomozygous592443187
3154516008154516009GA27GENIChomozygous592443188
3154516009154516010AT28GENIChomozygous592443189
3154516260154516261TC32GENIChomozygous592443190
3154516884154516885AG36GENIChomozygous592443191
3154517077154517078TC36GENIChomozygous594397566
3154517156154517157AG31GENIChomozygous592443192
3154517593154517594TC20GENIChomozygous592443193
3154517632154517633G-27GENIChomozygous725526782
3154517898154517899TC25GENIChomozygous592443194
3154517982154517986GGCA----23GENIChomozygous725526783
3154518068154518069GA30GENIChomozygous592443195
3154518158154518159TTA31GENIChomozygous725526784
3154518562154518563CT33GENIChomozygous594397567
3154518737154518738AG15GENIChomozygous592443196
3154518931154518932GGT20GENICpossibly homozygous725526785
3154519100154519101CT27GENIChomozygous594397568
3154519176154519177C-8GENICheterozygous725526786
3154519184154519185CCA8GENICpossibly homozygous725526787
3154519315154519316CT25GENIChomozygous592443197
3154519896154519897CCTT19GENIChomozygous725526790
3154519985154519986AG40GENIChomozygous592443198
3154520058154520059TC33GENIChomozygous592443199
3154520781154520782TC17GENIChomozygous592443200
3154520987154520988CT23GENIChomozygous592443201
3154521914154521915TTAA12GENIChomozygous725526792
3154521930154521931AAC11GENICheterozygous725526793
3154522134154522135AG32GENIChomozygous592443202