chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125743344125743345AT29GENICpossibly homozygous513615339
7125743354125743355CA26GENICpossibly homozygous513615340
7125744815125744816GA25GENIChomozygous513615341
7125745570125745580TGTGTGTGTA----------17GENIChomozygous687647175
7125745576125745580TGTA----19GENIChomozygous687647176
7125747420125747421GA17GENIChomozygous512774212
7125747647125747655CAACATGA--------15GENIChomozygous687647177
7125747731125747733TG--19GENIChomozygous687647178
7125748235125748236TC33GENIChomozygous512774213
7125748533125748534TC26GENIChomozygous513615342
7125748640125748641CG33GENICpossibly homozygous512774214
7125748702125748703CG40GENICheterozygous513615343
7125748724125748725AG42GENICheterozygous513615344
7125748861125748862CT28GENICheterozygous513615345
7125748927125748928GA21GENIChomozygous512774215
7125749414125749415AG28GENIChomozygous512774216
7125749577125749578GGGCAGTCAGTGCCC22GENIChomozygous687647179
7125749657125749658GT23GENIChomozygous513615346
7125751261125751262GA18GENIChomozygous513615347
7125752000125752001TC22GENIChomozygous512774217
7125753821125753822CT23GENICpossibly homozygous513615348
7125753897125753898CT23GENIChomozygous512774218
7125753949125753950GA28GENIChomozygous512774219
7125754274125754275AG19GENIChomozygous512774220
7125754320125754321CT27GENIChomozygous512774221
7125754367125754368CT33GENIChomozygous512774222
7125754379125754380GC32GENIChomozygous512774223
7125755157125755158GA33GENICpossibly homozygous512774224
7125755666125755667CT23GENIChomozygous512774225
7125755703125755704CT24GENIChomozygous512774226
7125756500125756501TC26GENIChomozygous512774227
7125756849125756850AG25GENIChomozygous512774228
7125756949125756950CCAAAA18GENICheterozygous687647180
7125756965125756966GGAAAA16GENIChomozygous687647181
7125757153125757154TTA20GENIChomozygous687647182