chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5119054319119054320GA16GENIChomozygous55663875
5119054330119054331CT17GENIChomozygous55663877
5119054761119054762TG19GENIChomozygous55663879
5119055350119055351A-12GENIChomozygous55663881
5119055369119055370GA16GENIChomozygous55663882
5119056193119056194AG14GENIChomozygous55663884
5119058417119058418GA17GENIChomozygous55663886
5119060466119060467CT9GENIChomozygous55663888
5119061102119061103AC11GENIChomozygous55663890
5119065461119065462AG17GENIChomozygous55663897
5119066304119066305T-16GENIChomozygous56121772
5119067159119067160TC14GENIChomozygous55663898
5119069262119069263CT17GENIChomozygous55663901
5119069269119069270GT16GENIChomozygous55663903