chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----21GENIChomozygous751448165
3154514276154514277TG22GENIChomozygous640712267
3154514414154514415AAGTCT12GENIChomozygous751448167
3154514475154514476TC15GENIChomozygous640712268
3154514477154514478TC15GENIChomozygous640712269
3154515475154515476GA11GENIChomozygous640712270
3154515681154515682TA25GENIChomozygous640712271
3154516008154516009GA29GENIChomozygous640712272
3154516009154516010AT32GENIChomozygous640712273
3154516260154516261TC21GENIChomozygous640712274
3154516884154516885AG32GENIChomozygous640712275
3154517077154517078TC20GENIChomozygous640712276
3154517156154517157AG14GENIChomozygous640712277
3154517593154517594TC25GENIChomozygous640712278
3154517632154517633G-19GENIChomozygous751448168
3154517898154517899TC21GENIChomozygous640712279
3154517982154517986GGCA----17GENIChomozygous751448169
3154518068154518069GA20GENIChomozygous640712280
3154518158154518159TTA17GENIChomozygous751448170
3154518562154518563CT13GENIChomozygous640712281
3154518737154518738AG12GENIChomozygous640712282
3154518931154518932GGT11GENICpossibly homozygous751448171
3154519100154519101CT10GENIChomozygous640712283
3154519184154519185CCA9GENIChomozygous751448172
3154519315154519316CT21GENIChomozygous640712284
3154519896154519897CCTT14GENICpossibly homozygous751448175
3154519985154519986AG12GENIChomozygous640712285
3154520058154520059TC21GENIChomozygous640712286
3154520781154520782TC24GENIChomozygous640712287
3154520987154520988CT32GENIChomozygous640712288
3154521914154521915TTAA5GENIChomozygous751448177
3154521930154521931AAC5GENICheterozygous751448178
3154522134154522135AG7GENIChomozygous640712289