chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4129549692129549700GGGAGGGA59GENIChomozygous131641869
4129551422129551423TG53GENIChomozygous119410923
4129551631129551632TC49GENIChomozygous119410924
4129552763129552764TC50GENIChomozygous113303896
4129553364129553365TC49GENIChomozygous119410925
4129553382129553383AG50GENIChomozygous119410926
4129554395129554396AT46GENIChomozygous113303898
4129558064129558065AG52GENIChomozygous113303899
4129560719129560720GA48GENIChomozygous119410927
4129561902129561903CT55GENIChomozygous119410928
4129562305129562306CT48GENIChomozygous119410929
4129562383129562384TC49GENIChomozygous113303904
4129563452129563453AT51GENIChomozygous119410930
4129563907129563908A51GENIChomozygous131641870
4129564136129564137GA61GENIChomozygous119410931
4129565029129565030TC23GENIChomozygous112826803
4129565923129565924GA50GENIChomozygous119410932
4129566251129566252AG60GENICpossibly homozygous119410933
4129567640129567641GC60GENIChomozygous119410934
4129552306129552307AG41GENIChomozygous113159944
4129554585129554586AG55GENIChomozygous113159945
4129558265129558266TC51GENIChomozygous113159947
4129569148129569150TT46GENIChomozygous128077457
4129569151129569152C47GENIChomozygous128077458
4129569156129569157C46GENIChomozygous128077459
4129569163129569164G51GENIChomozygous128077460
4129569212129569213C47GENIChomozygous128077464
4129569177129569178C50GENIChomozygous128077461
4129569189129569190G51GENIChomozygous128077462
4129569199129569201GC49GENIChomozygous128077463