chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155400557054005571TA18GENIChomozygous65114235
155400603154006032GA10GENIChomozygous66067546
155400638454006385TG12GENIChomozygous65114237
155400671054006711AC31GENIChomozygous65566786
155400755054007551GA16GENIChomozygous65566787
155400799754007998CT33GENIChomozygous65566788
155400816354008164CT19GENIChomozygous65566789
155400842054008421CA18GENIChomozygous65566790
155400896954008970TC18GENIChomozygous65566791
155401025754010258AG7GENIChomozygous65114243
155401184454011845GA12GENIChomozygous65566794
155401218654012187GA18GENIChomozygous65566795
155401248554012486CT10GENIChomozygous65114245
155401276954012770CT20GENIChomozygous65566796
155401284654012847TC21GENIChomozygous65566797
155401292254012923CT17GENIChomozygous65566798
155401436154014362GA7GENIChomozygous65114247
155401462854014629TC7GENIChomozygous65114248
155401522454015225TC20GENIChomozygous65114250
155401557154015572CT13GENIChomozygous65566799
155401580354015804TC12GENIChomozygous65114253
155401666554016666AT10GENIChomozygous65114257
155402107154021072CT16GENIChomozygous65114264
155402358654023587CT15GENIChomozygous65566801
155402409554024096AG12GENIChomozygous65114269
155402425454024255GA9GENIChomozygous65566802
155402427154024272TG15GENIChomozygous65566803
155402443654024437GC25GENIChomozygous65566804
155402555054025552AA13GENICheterozygous66067555
155402590754025908CT5GENIChomozygous65114272
155402680354026804AT5GENIChomozygous65114273
155402732854027330GG15GENICheterozygous65715135
155401234154012341C20GENIChomozygous66377732