chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887210140887211TG22GENIChomozygous811842763
4140887405140887406GC30GENIChomozygous811842764
4140887526140887527AG37GENIChomozygous811842765
4140889290140889291CA29GENICheterozygous811842766
4140892114140892115TA33GENIChomozygous811842767
4140892182140892183AT47GENICheterozygous811842768
4140893672140893673CA30GENICheterozygous811842769
4140894149140894150GA23GENIChomozygous811842770
4140894483140894484TC29GENIChomozygous811842771
4140894658140894659GC43GENIChomozygous811842772
4140896988140896989GA27GENIChomozygous811842773
4140899328140899329GA28GENIChomozygous811842774
4140901019140901020TC24GENICheterozygous811842775
4140902715140902716TC31GENIChomozygous811842776
4140902957140902958AG31GENIChomozygous811842777
4140903807140903808CT10GENIChomozygous811842778
4140904293140904294CG19GENICpossibly homozygous811842779
4140904305140904306TC14GENICpossibly homozygous811842780
4140906395140906396AG43GENIChomozygous811842781
4140907673140907674TC49GENICheterozygous811842782
4140908274140908275TG27GENIChomozygous811842783
4140908994140908995GC16GENIChomozygous811842784
4140909042140909043GA22GENIChomozygous811842785
4140909059140909060CA27GENIChomozygous811842786
4140909109140909110GA32GENIChomozygous811842787
4140909129140909130CT39GENICpossibly homozygous811842788
4140909170140909171GA37GENIChomozygous811842789
4140909196140909197CT35GENIChomozygous811842790
4140909244140909245GT33GENIChomozygous811842791
4140909248140909249TA32GENIChomozygous811842792
4140909269140909270GA35GENIChomozygous811842793
4140909286140909287GC35GENIChomozygous811842794
4140913023140913024AG20GENIChomozygous811842795
4140913522140913523CT21GENIChomozygous811842796
4140916630140916631TG20GENIChomozygous811842797
4140916631140916632CA20GENIChomozygous811842798
4140916937140916938GA32GENIChomozygous811842799