chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106605390066053901AAT8GENIChomozygous52382531
106605703666057037A-12GENICheterozygous52382533
106605860766058608CT11GENICpossibly homozygous52382535
106606008266060083GGA6GENICheterozygous51479041
106606008366060084A-6GENICheterozygous51479042
106606284766062848TC45GENIChomozygous51479043
106606541966065420CCTTTT20GENIChomozygous51479049
106606617866066179TTCTTCTGGAGTGTCTGAAGACAGTGACAGTGTAGTG12GENIChomozygous52382537
106606619066066191AACACACATTAAATAAATAAATAAATTTTTTTATTTAATGTGTGCGAGTACAAAGTCACT10GENIChomozygous52382539
106606639166066392GC9GENIChomozygous51479050
106606651466066515CCT4GENICheterozygous52440872
106606682466066825CCT5GENICheterozygous51479051
106606862366068624TG11GENIChomozygous51479055
106606867466068675T-7GENICheterozygous52440874
106606614166066142GT13GENIChomozygous51907720
106606896766068968AAT17GENIChomozygous51479056
106606930666069314AGAGAGGC--------2GENIChomozygous52382541
106606982166069822CT6GENIChomozygous51907722
106606983566069836A-2GENIChomozygous51479058
106607148266071483AAACAC12GENIChomozygous51479060
106607601666076017GGAA6GENIChomozygous51479068
106607671566076716CCTGTT24GENIChomozygous53027635
106607825666078257AATG19GENICpossibly homozygous51907726
106608150866081509CT25GENIChomozygous51907730