chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46210477062104771TG13GENICpossibly homozygous112671537
46211632162116321TT15GENIChomozygous128040835
46211632662116327A14GENIChomozygous128040836
46211633562116335A11GENIChomozygous128040837
46211634962116349A9GENIChomozygous128040838
46211636062116361C7GENIChomozygous128040839
46211636162116362CT7GENIChomozygous122054300
46211637062116372AG7GENIChomozygous128040840
46211637662116376T7GENIChomozygous128040841
46211637962116380CT7GENIChomozygous122054304
46211638362116384C6GENIChomozygous128040842
46211640662116407T1GENIChomozygous128040843
46211641062116410TA1GENIChomozygous128040844
46211641662116417AT1GENIChomozygous122054308
46211641862116418TTTATTATG1GENIChomozygous128040845
46211641962116420AC1GENIChomozygous122054310
46211642762116428C1GENIChomozygous128040846
46212015862120158A18GENIChomozygous128040851
46212295462122954C23GENIChomozygous128040861
46211199562111997TC11GENICheterozygous130752121
46211634662116347AC9GENIChomozygous119369872
46211634962116350TG9GENIChomozygous119369873
46222324962223251AC15GENICheterozygous130295670