chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1276312622276312623CG18GENIChomozygous120477613
1276313173276313174CT39GENIChomozygous108658713
1276313181276313182GA38GENIChomozygous120477614
1276313182276313183AG38GENIChomozygous120477615
1276313275276313276AT45GENIChomozygous108803355
1276313525276313526CT42GENIChomozygous108658715
1276313553276313554GA38GENIChomozygous120477616
1276313554276313555AG38GENIChomozygous108803359
1276313585276313586GA35GENIChomozygous108658716
1276360524276360525AC19GENIChomozygous108658746
1276402847276402848AG30GENIChomozygous108658781
1276478420276478421GA28GENIChomozygous108658914
1276478422276478423TA28GENIChomozygous108658915
1276478423276478424GC28GENIChomozygous108658916
1276505502276505503CG8GENIChomozygous108658967