chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99073346490733465GGT9GENIChomozygous818174840
99073349690733497GGT13GENIChomozygous818174841
99073603090736031TTGGGA19GENIChomozygous818174842
99073603290736033TG19GENIChomozygous818174843
99073687890736879TG15GENIChomozygous818174844
99073692190736922TG19GENIChomozygous818174845
99073693290736933TG19GENIChomozygous818174846
99073694690736947AG18GENIChomozygous818174847
99073695490736955TG17GENIChomozygous818174848
99073697190736972TA16GENIChomozygous818174849
99073838490738385CT9GENIChomozygous818174850
99073856290738563TC11GENIChomozygous818174851
99073864990738650CT8GENIChomozygous818174852
99074061090740612AT--8GENIChomozygous818174853
99074067290740673CT9GENIChomozygous818174854
99074122690741228TG--10GENICheterozygous818174855
99074145590741456AAAGG9GENIChomozygous818174856
99074148190741482TA8GENIChomozygous818174857
99074148690741487GA7GENIChomozygous818174858
99074155290741553TG7GENIChomozygous818174859
99074164490741645AG7GENIChomozygous818174860
99074166290741663TC7GENIChomozygous818174861
99074258390742584CT9GENIChomozygous818174862
99074258590742586TC9GENIChomozygous818174863
99074259990742600CA10GENIChomozygous818174864
99074260190742602GT10GENIChomozygous818174865
99074260490742606CC--10GENIChomozygous818174866
99074261090742611CT10GENIChomozygous818174867
99074261190742612CA11GENIChomozygous818174868
99074293790742938CG11GENIChomozygous818174869
99074294190742943AG--11GENIChomozygous818174870
99074294590742946AAGG11GENIChomozygous818174871
99074296990742970GA12GENIChomozygous818174872
99074298290742983CT12GENIChomozygous818174873
99074300390743004GA13GENIChomozygous818174874
99074301090743011GA13GENIChomozygous818174875
99074305590743056CT10GENIChomozygous818174876
99074305690743057CT10GENIChomozygous818174877
99074307290743073AG9GENIChomozygous818174878
99074769090747691TTAG9GENIChomozygous818174879