chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75363102053631021TG13GENIChomozygous115685774
75363131853631319TG20GENIChomozygous118308817
75363296753632968AG19GENIChomozygous115685776
75363369553633696TC15GENIChomozygous115685777
75363422253634223AG14GENIChomozygous115685778
75363454853634549CT19GENIChomozygous118308818
75363573753635738CT21GENICpossibly homozygous118308819
75363753153637537ACAGAC14GENICheterozygous131014819
75363164853631648A16GENIChomozygous131678286
75363929453639295GT18GENIChomozygous115685793
75363963053639631CT15GENIChomozygous118308820
75364237953642380GA18GENIChomozygous118308821
75364584453645845AG15GENIChomozygous115685803
75364864553648646AC27GENIChomozygous116290120
75364745753647458TC25GENIChomozygous118308822
75364771753647718TC23GENIChomozygous116166389
75364828453648285AG17GENIChomozygous115685806
75364859853648599GA20GENIChomozygous118308823
75364868153648682CT30GENIChomozygous116290121
75364901953649020GA19GENIChomozygous118370162