chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3124871209124871210GA19GENIChomozygous111694921
3124872268124872269CA24GENIChomozygous119651488
3124872270124872271TC24GENIChomozygous112027739
3124873116124873117AC27GENICpossibly homozygous111694925
3124873548124873549CA11GENIChomozygous111694926
3124873588124873589CT22GENIChomozygous111694928
3124873871124873872CT15GENIChomozygous111694929
3124873899124873900AG18GENIChomozygous111694931
3124874137124874138TC20GENIChomozygous111694932
3124874520124874521TC20GENIChomozygous111694936
3124875011124875012AC19GENIChomozygous111694937
3124875533124875534GA19GENIChomozygous111694941
3124875940124875941AG12GENIChomozygous111694944