chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5126534920126534921TA9GENIChomozygous126202930
5126540260126540261AG6GENIChomozygous126202931
5126560804126560805CG9GENIChomozygous126202932
5126560843126560844CT6GENIChomozygous126202933
5126564322126564323CT3GENICheterozygous126217543
5126569047126569048AG9GENIChomozygous126202937
5126598698126598699CT7GENIChomozygous126202939
5126598720126598721CT9GENIChomozygous126202940
5126598743126598744CT9GENIChomozygous126202941
5126598900126598901CT16GENIChomozygous126202942
5126598935126598936CT12GENIChomozygous126202943
5126598970126598971AC12GENIChomozygous126202944
5126601268126601269CG8GENIChomozygous126217545
5126601269126601270GT8GENICheterozygous126217546
5126601269126601270GT8GENICheterozygous126217548
5126601270126601271TA11GENIChomozygous126217550
5126621922126621923TG11GENIChomozygous126202946
5126621933126621934TG11GENIChomozygous126202947
5126621941126621942TG10GENIChomozygous126202948
5126621985126621986TA7GENIChomozygous126202949
5126622048126622049TA5GENIChomozygous126202950
5126648675126648676GA5GENICheterozygous126217551