chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266866964266866965TG33GENIChomozygous801786175
1266867306266867307GA15GENIChomozygous801786176
1266869171266869172TC18GENIChomozygous801786177
1266869354266869355CT15GENIChomozygous801786178
1266871195266871196CT36GENIChomozygous801786179
1266871799266871800AG14GENIChomozygous801786180
1266872295266872296GA29GENIChomozygous801786181
1266875889266875890TC25GENICheterozygous801786182
1266876378266876379AG32GENIChomozygous801786183
1266876812266876813GA29GENIChomozygous801786184
1266878355266878356CT24GENIChomozygous801786185
1266879795266879796TG23GENIChomozygous801786186
1266879804266879805AG20GENIChomozygous801786187
1266881234266881235CT37GENIChomozygous801786188
1266881721266881722AG24GENIChomozygous801786189
1266882385266882386GC24GENIChomozygous801786190
1266884148266884149CG23GENIChomozygous801786191
1266885292266885293AC21GENIChomozygous801786192
1266885604266885605GA26GENIChomozygous801786193
1266885897266885898TC15GENIChomozygous801786194
1266886280266886281GT10GENIChomozygous801786195
1266886544266886545GC40GENICheterozygous801786196
1266886574266886575TG51GENICheterozygous801786197
1266886853266886854GT40GENICheterozygous801786198
1266886862266886863TG47GENICheterozygous801786199
1266887077266887078GA20GENIChomozygous801786200
1266888529266888530CT22GENIChomozygous801786201
1266889651266889652TC18GENIChomozygous801786202
1266890046266890047TC35GENIChomozygous801786203
1266892512266892513TC24GENIChomozygous801786204
1266894775266894776GA26GENIChomozygous801786205
1266895476266895477AG33GENIChomozygous801786206
1266896747266896748TG25GENIChomozygous801786207
1266897388266897389TC17GENIChomozygous801786208
1266897506266897507GA21GENICpossibly homozygous801786209
1266898357266898358AG24GENIChomozygous801786210
1266898962266898963GA13GENIChomozygous801786211
1266899513266899514GA39GENIChomozygous801786212
1266907705266907706AT32GENIChomozygous801786213