chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155400557054005571TA20GENIChomozygous65114235
155400603154006032GA18GENIChomozygous66067546
155400638454006385TG12GENIChomozygous65114237
155400990954009910AC18GENIChomozygous65566792
155400671054006711AC30GENIChomozygous65566786
155400755054007551GA18GENIChomozygous65566787
155400799754007998CT26GENICpossibly homozygous65566788
155400816354008164CT11GENIChomozygous65566789
155400842054008421CA17GENIChomozygous65566790
155400896954008970TC23GENIChomozygous65566791
155400991054009911GT19GENIChomozygous65566793
155401025754010258AG16GENIChomozygous65114243
155401184454011845GA12GENIChomozygous65566794
155401218654012187GA23GENIChomozygous65566795
155401248554012486CT20GENIChomozygous65114245
155401276954012770CT24GENIChomozygous65566796
155401284654012847TC22GENICpossibly homozygous65566797
155401292254012923CT23GENIChomozygous65566798
155401436154014362GA17GENIChomozygous65114247
155401522454015225TC31GENIChomozygous65114250
155401557154015572CT17GENIChomozygous65566799
155401580354015804TC12GENIChomozygous65114253
155401601454016015CT17GENIChomozygous65566800
155401666554016666AT14GENIChomozygous65114257
155402107154021072CT16GENIChomozygous65114264
155402358654023587CT25GENIChomozygous65566801
155402409554024096AG25GENIChomozygous65114269
155402425454024255GA28GENIChomozygous65566802
155402427154024272TG30GENIChomozygous65566803
155402443654024437GC24GENIChomozygous65566804
155402498354024984TC15GENIChomozygous65566805
155402590754025908CT19GENIChomozygous65114272
155402680354026804AT15GENIChomozygous65114273
155402680654026807AT14GENIChomozygous65566806
155401456254014563TC20GENIChomozygous65969760
155401456354014564CA20GENIChomozygous84112619