chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4181482263181482264AG32GENIChomozygous113567389
4181482730181482731CT10GENIChomozygous113567390
4181483278181483279AG8GENIChomozygous112976692
4181486377181486378AG17GENIChomozygous113567397
4181486529181486530CT11GENIChomozygous113567398
4181486530181486531CT11GENIChomozygous113567399
4181488066181488067TG5GENIChomozygous112976707
4181488564181488565TC8GENIChomozygous112976711
4181489023181489024TC21GENIChomozygous112976712
4181489147181489148GA24GENIChomozygous113567401
4181489455181489456TG18GENIChomozygous113567402
4181490273181490274GA21GENIChomozygous113567403
4181490652181490653TC23GENIChomozygous113567404
4181492830181492831AC25GENIChomozygous112976726
4181493603181493604TC13GENIChomozygous112976729
4181493746181493747GA23GENIChomozygous112976730
4181493997181493998TC10GENIChomozygous112976731
4181493998181493999TC10GENIChomozygous112976732
4181495702181495703GA19GENIChomozygous113567405
4181496494181496495GA13GENIChomozygous113567406
4181496748181496749TC17GENIChomozygous113567407
4181497022181497023CA18GENIChomozygous112976742
4181497250181497251GT12GENIChomozygous112976744
4181498830181498831GA13GENIChomozygous113567408
4181499837181499838GA11GENIChomozygous112976757
4181501326181501327AC17GENIChomozygous112976759
4181502350181502351CA22GENIChomozygous113567409