chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103580173535801735A48GENIChomozygous131090877
103580315635803157TC72GENIChomozygous116758103
103580595535805956TC42GENIChomozygous116758105
103580934435809345AT66GENIChomozygous116558488
103580934635809347CT65GENIChomozygous116558490
103580936235809363C60GENIChomozygous128807425
103580936435809365CA57GENIChomozygous116558492
103580941335809414C57GENIChomozygous128807426
103580942935809430A55GENIChomozygous128807427
103581039835810398G44GENIChomozygous128807428
103581089635810897GA67GENIChomozygous116758107
103581273035812731A30GENICpossibly homozygous128807429
103582457335824574C44GENICheterozygous130576509
103582930835829309A44GENIChomozygous128807438
103582937535829376T52GENIChomozygous131090878
103583033635830337GC42GENICheterozygous132332833
103581359235813593AT11GENICheterozygous123341281
103581732935817330AG26GENIChomozygous117988690
103582416235824163CT52GENIChomozygous116558520
103582653435826535TC49GENIChomozygous116558522
103583033535830336GC42GENICheterozygous132332832
103583012935830130AG46GENIChomozygous116924894
103583097735830978AC65GENIChomozygous116558528
103583156135831562CT41GENIChomozygous116558530
103583365035833651TA61GENIChomozygous116558536