chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46210477062104771TG14GENICpossibly homozygous112671537
46211632162116321TT16GENIChomozygous128040835
46211632662116327A16GENIChomozygous128040836
46211633562116335A14GENIChomozygous128040837
46211634662116347AC14GENIChomozygous119369872
46211634962116350TG14GENIChomozygous119369873
46211634962116349A14GENIChomozygous128040838
46211636062116361C12GENIChomozygous128040839
46211636162116362CT12GENIChomozygous122054300
46211637062116372AG10GENIChomozygous128040840
46211637662116376T9GENIChomozygous128040841
46211637962116380CT8GENIChomozygous122054304
46211638362116384C8GENIChomozygous128040842
46211640662116407T6GENIChomozygous128040843
46211641062116410TA6GENIChomozygous128040844
46211641662116417AT5GENIChomozygous122054308
46211641862116418TTTATTATG5GENIChomozygous128040845
46211641962116420AC5GENIChomozygous122054310
46211642762116428C4GENIChomozygous128040846
46211643862116438T1GENIChomozygous128040847
46212015862120158A17GENIChomozygous128040851
46212295462122954C23GENIChomozygous128040861
46222750362227504A7GENICheterozygous130648606