chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104081615540816156AT11GENICheterozygous116764756
104081652540816526AG10GENIChomozygous116570641
104082003140820032AG9GENIChomozygous116764758
104082038440820385CG9GENIChomozygous116764760
104082073640820737GC7GENIChomozygous116570688
104082140940821410CG3GENIChomozygous116764762
104082148040821481TC6GENIChomozygous116570690
104082212540822126TC7GENIChomozygous116764764
104082292240822923TG10GENIChomozygous116570694
104082325740823258GA9GENIChomozygous116570696
104082364440823645AG7GENIChomozygous116764766
104082364740823648AG7GENIChomozygous116764768
104082365040823651AG7GENIChomozygous116764770
104082517540825176CA5GENIChomozygous116570698
104082699740826998AT13GENIChomozygous116570706
104082880240828803TC8GENIChomozygous116570708
104083053840830539AT11GENIChomozygous116764772
104083124740831248AG14GENIChomozygous116570716
104083193540831936AG9GENIChomozygous116570718
104083301540833016CT7GENIChomozygous116570720
104083363440833635CT17GENIChomozygous116764774
104083388040833881CT14GENIChomozygous116570722
104083604440836045GA10GENIChomozygous116764776
104083671140836712CG9GENIChomozygous116570724
104083714440837145CT10GENIChomozygous116570726
104083784940837850GT14GENIChomozygous116570728
104083911340839114GT7GENIChomozygous116570730
104083939740839398TC7GENIChomozygous116570732
104083990240839903TC14GENIChomozygous116570736
104083990440839905AG14GENIChomozygous116570738
104084087140840872CG7GENIChomozygous116570744
104084326540843266CA6GENIChomozygous116570746
104084469840844699AG4GENIChomozygous116570748
104084535640845357AT15GENIChomozygous116570752