chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186025758960257590TC20GENIChomozygous110367737
186025765360257654GA28GENIChomozygous110367739
186025767560257676CT30GENIChomozygous110367741
186025841160258412GC33GENIChomozygous110631899
186025907460259075TA27GENIChomozygous110367749
186025956360259564AT31GENIChomozygous110367751
186025964760259648AG33GENIChomozygous110367755
186025967760259678GA27GENIChomozygous110631901
186025974760259748CT27GENIChomozygous110631903
186026016560260166AC30GENIChomozygous110703348
186026135060261351GC16GENIChomozygous110631905
186026341360263414AG30GENIChomozygous110775695
186026400160264002TG33GENIChomozygous110367763
186026401260264013GT28GENIChomozygous110631907
186026496260264963GT19GENIChomozygous110367765
186026540060265401TC26GENIChomozygous110367767
186026568660265687TC28GENIChomozygous110367770
186026571460265715AG29GENIChomozygous110367772
186026608360266084GT24GENICpossibly homozygous110367774
186026795660267957CA26GENIChomozygous110631909
186026796660267967GT22GENIChomozygous110367780
186026866360268664CG20GENIChomozygous110367782
186026904560269046TC20GENIChomozygous110367784
186026908660269087AG22GENIChomozygous110367786
186027028060270281GC19GENIChomozygous110480766
186027124760271248GA26GENIChomozygous110480768
186027224660272247GT34GENIChomozygous110480770
186027328260273283CG27GENIChomozygous110367794
186027726460277265AG26GENIChomozygous110480772
186028086660280867TA19GENIChomozygous110367808
186028094860280949GA19GENIChomozygous110367810
186027328660273287TG28GENIChomozygous110687580
186026348860263489CT18GENICheterozygous119554173
186026720560267206CT24GENICheterozygous119554174
186026721460267215CT20GENICpossibly homozygous119554175
186027321060273211AC11GENIChomozygous119496346
186027338260273383AC12GENIChomozygous119496347