chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5136148354136148355AG21GENIChomozygous137630814
5136149155136149156GC16GENIChomozygous137630815
5136150576136150577AC12GENIChomozygous137630816
5136151257136151258CT28GENIChomozygous137630817
5136152232136152233AG20GENIChomozygous137630818
5136152914136152915AT18GENIChomozygous137630819
5136153151136153152CT16GENIChomozygous137630820
5136154094136154095GA17GENIChomozygous137630821
5136154561136154562TG14GENIChomozygous137630822
5136155504136155504A13GENIChomozygous137344052
5136156331136156332AG22GENIChomozygous137630823
5136156407136156408TC25GENIChomozygous137630824
5136160420136160421TC14GENIChomozygous137630826
5136160514136160515TG21GENIChomozygous137630827
5136160930136160931CT12GENIChomozygous137630828
5136161535136161536CG12GENIChomozygous137630829
5136164915136164916GA10GENIChomozygous137630830
5136165066136165067GA17GENIChomozygous137630831
5136166214136166215TG24GENIChomozygous137630832
5136166239136166240AG28GENIChomozygous137630833
5136166418136166419TC16GENIChomozygous137630834
5136166940136166941AG19GENIChomozygous137630835
5136167466136167467GA20GENIChomozygous137630836
5136158249136158250T12GENICheterozygous403159418
5136158249136158250TC12GENIChomozygous154326991