chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103580173535801735A20GENICpossibly homozygous131090877
103580315635803157TC26GENIChomozygous116758103
103580595535805956TC15GENIChomozygous116758105
103580934435809345AT29GENIChomozygous116558488
103580934635809347CT28GENIChomozygous116558490
103580936235809363C23GENIChomozygous128807425
103580936435809365CA23GENIChomozygous116558492
103580941335809414C24GENIChomozygous128807426
103580942935809430A23GENIChomozygous128807427
103581039835810398G14GENIChomozygous128807428
103581089635810897GA22GENIChomozygous116758107
103581273035812731A6GENIChomozygous128807429
103581359235813593AT4GENIChomozygous123341281
103581732935817330AG9GENIChomozygous117988690
103582416235824163CT15GENIChomozygous116558520
103582653435826535TC26GENIChomozygous116558522
103582930835829309A13GENIChomozygous128807438
103582937535829376T21GENIChomozygous131090878
103583041735830417AAGCGC15GENICheterozygous128807440
103583097735830978AC23GENIChomozygous116558528
103583156135831562CT10GENIChomozygous116558530
103583365035833651TA20GENIChomozygous116558536
103583012935830130AG13GENIChomozygous116924894
103583041035830411GA13GENICpossibly homozygous117409467