chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2119129352119129353TG46GENIChomozygous109994880
2119129928119129929TC47GENIChomozygous109994882
2119131472119131473CA32GENIChomozygous109994884
2119132298119132299TA10GENIChomozygous109994886
2119133279119133280TC23GENIChomozygous109994888
2119134559119134560CT68GENIChomozygous109994890
2119135046119135047CT27GENIChomozygous109994892
2119135075119135076TG26GENIChomozygous109994894
2119135400119135401GA19GENIChomozygous109994896
2119135667119135668GA32GENIChomozygous109994898
2119135883119135884AT32GENIChomozygous109994900
2119135929119135930CT37GENIChomozygous109994902
2119136339119136340AG32GENIChomozygous109994904
2119137039119137040TC15GENIChomozygous109994906
2119137056119137057TC18GENIChomozygous109994908
2119137155119137156GA48GENIChomozygous109994910
2119137197119137198GA57GENIChomozygous109994912
2119137338119137339TC29GENIChomozygous109994914
2119137469119137470CT14GENIChomozygous109994915
2119137483119137484AG20GENIChomozygous109994917
2119137792119137793TC21GENIChomozygous109994919
2119137954119137955AT20GENIChomozygous109994921
2119138888119138889GA21GENIChomozygous109994923
2119138961119138962TC28GENIChomozygous109994925
2119139443119139444AT43GENIChomozygous109994927