chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----18GENIChomozygous735135241
3154514276154514277TG22GENIChomozygous609690148
3154514414154514415AAGTCT26GENIChomozygous735135243
3154514475154514476TC24GENIChomozygous609690149
3154514477154514478TC24GENIChomozygous609690150
3154515475154515476GA19GENIChomozygous609690151
3154515681154515682TA28GENIChomozygous609690152
3154516008154516009GA30GENIChomozygous609690153
3154516009154516010AT30GENIChomozygous609690154
3154516260154516261TC27GENIChomozygous609690155
3154516884154516885AG27GENIChomozygous609690156
3154517077154517078TC36GENIChomozygous611624357
3154517156154517157AG22GENIChomozygous609690157
3154517593154517594TC16GENIChomozygous609690158
3154517632154517633G-22GENIChomozygous735135244
3154517898154517899TC27GENIChomozygous609690159
3154517982154517986GGCA----31GENIChomozygous735135245
3154518068154518069GA40GENIChomozygous609690160
3154518158154518159TTA33GENIChomozygous735135246
3154518562154518563CT30GENIChomozygous611624358
3154518737154518738AG33GENIChomozygous609690161
3154518931154518932GGT19GENIChomozygous735135247
3154519100154519101CT22GENIChomozygous611624359
3154519184154519185CCA17GENIChomozygous735135248
3154519315154519316CT36GENIChomozygous609690162
3154519896154519897CCTT25GENICpossibly homozygous735135251
3154519985154519986AG32GENIChomozygous609690163
3154520058154520059TC33GENIChomozygous609690164
3154520781154520782TC29GENIChomozygous609690165
3154520987154520988CT27GENIChomozygous609690166
3154521914154521915TTAA10GENICpossibly homozygous735135253
3154521930154521931AAC4GENICheterozygous735135254
3154522134154522135AG19GENIChomozygous609690167