chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125743344125743345AT4GENICheterozygous597607890
7125743354125743355CA4GENICheterozygous597607891
7125744815125744816GA15GENICpossibly homozygous597607892
7125747094125747095CT22GENICheterozygous597097186
7125747095125747096CT21GENICheterozygous597097187
7125747420125747421GA29GENIChomozygous597097188
7125747534125747535CT24GENICpossibly homozygous597097189
7125747647125747655CAACATGA--------3GENICheterozygous727207793
7125747681125747682TG16GENICpossibly homozygous597097190
7125747731125747733TG--19GENIChomozygous727207794
7125748235125748236TC25GENICpossibly homozygous597097191
7125748533125748534TC31GENICpossibly homozygous597607893
7125748640125748641CG3GENICheterozygous597097192
7125748927125748928GA29GENIChomozygous597097193
7125749414125749415AG18GENIChomozygous597097194
7125749577125749578GGGCAGTCAGTGCCC3GENIChomozygous727207795
7125749657125749658GT21GENIChomozygous597607894
7125751261125751262GA23GENICpossibly homozygous597607895
7125752000125752001TC21GENIChomozygous597097195
7125753897125753898CT5GENIChomozygous597097196
7125753949125753950GA10GENIChomozygous597097197
7125754274125754275AG27GENIChomozygous597097198
7125754320125754321CT11GENIChomozygous597097199
7125754367125754368CT15GENICpossibly homozygous597097200
7125754379125754380GC12GENIChomozygous597097201
7125755157125755158GA8GENICheterozygous597097202
7125755666125755667CT15GENICpossibly homozygous597097203
7125755703125755704CT24GENIChomozygous597097204
7125756500125756501TC17GENIChomozygous597097205
7125756849125756850AG12GENICheterozygous597097206
7125757153125757154TTA1GENIChomozygous727207796