chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155400557054005571TA27GENIChomozygous65114235
155400575754005758GC27GENIChomozygous65654670
155400638454006385TG24GENIChomozygous65114237
155400663354006634GA31GENICpossibly homozygous65654672
155400927354009274GA26GENICpossibly homozygous65654676
155400990954009910AC26GENIChomozygous65566792
155400671054006711AC35GENIChomozygous65566786
155400799754007998CT56GENIChomozygous65566788
155400816354008164CT54GENIChomozygous65566789
155400842054008421CA31GENIChomozygous65566790
155400896954008970TC22GENIChomozygous65566791
155400677954006780GA28GENICpossibly homozygous66276322
155400991054009911GT24GENIChomozygous65566793
155401025754010258AG14GENIChomozygous65114243
155401184454011845GA31GENIChomozygous65566794
155401231554012316GA28GENICpossibly homozygous65654678
155401248554012486CT33GENIChomozygous65114245
155401267854012679AT32GENICpossibly homozygous65654680
155401284654012847TC37GENIChomozygous65566797
155401292254012923CT34GENIChomozygous65566798
155401436154014362GA33GENIChomozygous65114247
155401522454015225TC46GENIChomozygous65114250
155401564954015650AC26GENIChomozygous65654682
155401580354015804TC32GENIChomozygous65114253
155401666554016666AT23GENIChomozygous65114257
155401800854018009AT32GENICpossibly homozygous65114259
155402107154021072CT23GENIChomozygous65114264
155402288354022884CT32GENICpossibly homozygous65654688
155402297254022973GA34GENICpossibly homozygous65654690
155402507454025075GA13GENICpossibly homozygous65654692
155402590754025908CT22GENICpossibly homozygous65114272
155402680354026804AT28GENIChomozygous65114273
155402680654026807AT30GENICheterozygous65566806
155401456254014563TC21GENIChomozygous65969760
155401456354014564CA21GENIChomozygous84112619