chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118743511387435114CG42GENICpossibly homozygous51030158
118743517787435178AG9GENIChomozygous51030159
118743518687435187TC6GENICheterozygous51030160
118743522387435224TC9GENICheterozygous51030161
118743526187435262AAAT10GENICheterozygous51030162
118743526787435268AG9GENIChomozygous51030163
118743527387435274AG9GENIChomozygous51030164
118743561187435612AAAT12GENIChomozygous51030165
118743561787435618AG12GENIChomozygous51030166
118743562387435624AG13GENIChomozygous51030167
118743562587435626CT13GENICheterozygous51030168
118743563287435633AG16GENICheterozygous51030169
118743564287435643GA18GENICheterozygous51030170
118743565787435658CT22GENICheterozygous51030171
118743566087435661TC18GENIChomozygous51030172
118743568387435684CG26GENIChomozygous51030173
118743587987435880CG46GENIChomozygous51030174
118743601087436011CT39GENIChomozygous51030175
118743605587436056TC48GENIChomozygous51030176
118743660387436604GA48GENIChomozygous51030177
118743751687437517TC14GENICheterozygous51030178
118743751887437519GA14GENICheterozygous51030179
118743752287437523GA12GENICheterozygous51030180
118743824087438241CT48GENIChomozygous51030181
118743854687438547GA40GENIChomozygous51030182
118743996987439970AG36GENICheterozygous51030183
118744040187440402AG11GENICheterozygous51131153
118744056987440570AG33GENICheterozygous51030184
118744070587440706GGA21GENIChomozygous50857619
118744090487440905TC62GENICheterozygous51030185
118744113787441138GA57GENIChomozygous51030186
118744204387442044CG57GENIChomozygous51030187
118744223587442236GA52GENIChomozygous51030188
118744240387442404A-21GENIChomozygous51030189
118744271487442719TAATC-----37GENIChomozygous51030190
118744293687442942TGTGTT------15GENICheterozygous51030191
118744294087442942TT--15GENICheterozygous51030192
118744296187442962GT18GENICheterozygous51131165
118744052187440522AG18GENICheterozygous51131156
118744294987442950GT19GENICheterozygous51131159
118744295787442958CG18GENICheterozygous51131162
118744303987443065TGTGTGTGTGTGTGTGCGTGCGTGCA--------------------------8GENICpossibly homozygous51030193
118744321987443220TC37GENIChomozygous51030194
118744322087443221TC39GENIChomozygous51030195
118744437187444372TC61GENICpossibly homozygous51030196