chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97066280570662806GA27INTERGENIChomozygous68485040
97066417870664179AC22INTERGENIChomozygous68485043
97066590870665909AG21INTERGENICpossibly homozygous68485045
97066654270666543AG25INTERGENIChomozygous68485048
97066669470666695GT21INTERGENIChomozygous68485050
97066986770669868TC31INTERGENICpossibly homozygous68485053
97067265070672651TC28INTERGENIChomozygous68485056
97067807770678078AG19GENIChomozygous68485060
97067824870678249TC16GENIChomozygous68485063
97068094970680950TG21GENIChomozygous82514642
97068095070680951GT21GENIChomozygous82514643
97068417070684171AG32GENIChomozygous68485066
97068497770684978AG31GENIChomozygous68485069
97068649870686499TA30GENIChomozygous68485072
97068778570687786CG27GENIChomozygous68485075
97066863570668636GA13INTERGENICheterozygous68141180