chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97066158870661589CT27INTERGENIChomozygous69007660
97066559270665593CA29INTERGENIChomozygous69007663
97066590870665909AG18INTERGENIChomozygous68485045
97066654270666543AG25INTERGENICpossibly homozygous68485048
97066669470666695GT25INTERGENIChomozygous68485050
97066784870667849GA30INTERGENICpossibly homozygous69007666
97066982170669822GC32INTERGENIChomozygous69007675
97066986770669868TC25INTERGENIChomozygous68485053
97067265070672651TC29INTERGENICpossibly homozygous68485056
97067412670674127CT23INTERGENIChomozygous69007678
97067566070675661TC26INTERGENIChomozygous69007681
97067807770678078AG28GENICpossibly homozygous68485060
97067824870678249TC18GENIChomozygous68485063
97067941970679420GC24GENIChomozygous69007684
97068417070684171AG15GENIChomozygous68485066
97068463770684638AT16GENIChomozygous69007687
97068649870686499TA24GENIChomozygous68485072
97067673470676735TC12INTERGENIChomozygous69215931
97067675870676759GC15GENIChomozygous69215932