chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5136148354136148355AG65GENIChomozygous137630814
5136149155136149156GC64GENIChomozygous137630815
5136150576136150577AC48GENIChomozygous137630816
5136151257136151258CT60GENIChomozygous137630817
5136152232136152233AG62GENICpossibly homozygous137630818
5136152914136152915AT39GENICpossibly homozygous137630819
5136153151136153152CT57GENIChomozygous137630820
5136154094136154095GA55GENIChomozygous137630821
5136154561136154562TG55GENIChomozygous137630822
5136155504136155504A55GENICpossibly homozygous137344052
5136156331136156332AG59GENIChomozygous137630823
5136156407136156408TC49GENIChomozygous137630824
5136160420136160421TC66GENIChomozygous137630826
5136160514136160515TG52GENIChomozygous137630827
5136160930136160931CT61GENIChomozygous137630828
5136161535136161536CG50GENIChomozygous137630829
5136164915136164916GA51GENIChomozygous137630830
5136165066136165067GA54GENIChomozygous137630831
5136166214136166215TG54GENIChomozygous137630832
5136166239136166240AG55GENIChomozygous137630833
5136166418136166419TC47GENIChomozygous137630834
5136166940136166941AG46GENIChomozygous137630835
5136167466136167467GA51GENIChomozygous137630836
5136158249136158250TC38GENIChomozygous154326991
5136158249136158250T38GENICheterozygous403159418