chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155540716955407170AG22GENIChomozygous112686812
155540742455407425CT29GENIChomozygous112686814
155540759855407599CT22GENIChomozygous112686816
155540763255407633GA21GENIChomozygous112686818
155540829755408298AG16GENIChomozygous112686820
155540839455408395GA16GENIChomozygous112686822
155540880355408804GT17GENIChomozygous112686824
155540907455409075GA23GENIChomozygous112686826
155541020955410210TC13GENIChomozygous112686827
155541133455411335GC15GENIChomozygous112686829
155541156755411568CG13GENIChomozygous112686831
155541166055411661CT17GENIChomozygous112686833
155541236455412365TC18GENIChomozygous112686835
155541292055412921CG12GENIChomozygous112686837
155541292155412922GA12GENIChomozygous112515369
155541396155413962TC18GENIChomozygous112515375
155541426455414265CT33GENIChomozygous112686839
155541509655415097CA16GENIChomozygous112686841
155541535555415356TC31GENIChomozygous112686843
155541564055415641CA22GENIChomozygous112686845
155541658255416583GA21GENIChomozygous112515381
155541664455416645TC15GENIChomozygous112515383
155541330955413310CT21GENIChomozygous113143555