chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103580173535801735A30GENIChomozygous131090877
103580315635803157TC45GENIChomozygous116758103
103580595535805956TC38GENIChomozygous116758105
103580934435809345AT55GENIChomozygous116558488
103580934635809347CT55GENIChomozygous116558490
103580936235809363C53GENIChomozygous128807425
103580936435809365CA52GENIChomozygous116558492
103580941335809414C53GENIChomozygous128807426
103580942935809430A55GENIChomozygous128807427
103581039835810398G27GENIChomozygous128807428
103581089635810897GA41GENIChomozygous116758107
103581273035812731A23GENICpossibly homozygous128807429
103581359235813593AT7GENIChomozygous123341281
103581732935817330AG14GENIChomozygous117988690
103582416235824163CT41GENIChomozygous116558520
103582653435826535TC42GENIChomozygous116558522
103582930835829309A33GENIChomozygous128807438
103582937535829376T37GENIChomozygous131090878
103583097735830978AC28GENIChomozygous116558528
103583156135831562CT32GENIChomozygous116558530
103583238535832385GGGGCTGGG27GENICheterozygous133757514
103583238835832388TTAGCTCAGTGGTAGAGCGCTT26GENICheterozygous133757515
103583239035832390CTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAG15GENICheterozygous133757516
103583365035833651TA49GENIChomozygous116558536
103583012935830130AG34GENIChomozygous116924894
103583033535830336GC18GENICheterozygous132332832
103583033635830337GC18GENICheterozygous132332833