chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155400557054005571TA34GENIChomozygous65114235
155400575754005758GC34GENIChomozygous65654670
155400638454006385TG29GENIChomozygous65114237
155400663354006634GA43GENIChomozygous65654672
155400927354009274GA37GENIChomozygous65654676
155400990954009910AC34GENIChomozygous65566792
155400816354008164CT51GENIChomozygous65566789
155400671054006711AC39GENIChomozygous65566786
155400799754007998CT57GENIChomozygous65566788
155400842054008421CA34GENIChomozygous65566790
155400896954008970TC25GENIChomozygous65566791
155400677954006780GA41GENIChomozygous66276322
155400991054009911GT32GENIChomozygous65566793
155401025754010258AG17GENIChomozygous65114243
155401184454011845GA29GENIChomozygous65566794
155401231554012316GA24GENIChomozygous65654678
155401248554012486CT28GENIChomozygous65114245
155401267854012679AT36GENIChomozygous65654680
155401284654012847TC30GENIChomozygous65566797
155401292254012923CT29GENIChomozygous65566798
155401436154014362GA36GENIChomozygous65114247
155401522454015225TC39GENIChomozygous65114250
155401564954015650AC43GENIChomozygous65654682
155401580354015804TC24GENIChomozygous65114253
155401666554016666AT38GENIChomozygous65114257
155401800854018009AT39GENIChomozygous65114259
155402107154021072CT35GENIChomozygous65114264
155402288354022884CT42GENIChomozygous65654688
155402297254022973GA30GENIChomozygous65654690
155402507454025075GA33GENIChomozygous65654692
155402590754025908CT29GENIChomozygous65114272
155402680354026804AT31GENIChomozygous65114273
155401456254014563TC39GENIChomozygous65969760
155401456354014564CA38GENIChomozygous84112619