chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97066158870661589CT36INTERGENIChomozygous69007660
97066559270665593CA34INTERGENIChomozygous69007663
97066590870665909AG29INTERGENIChomozygous68485045
97066654270666543AG41INTERGENIChomozygous68485048
97066669470666695GT41INTERGENIChomozygous68485050
97066784870667849GA32INTERGENIChomozygous69007666
97066982170669822GC27INTERGENIChomozygous69007675
97066986770669868TC29INTERGENIChomozygous68485053
97067265070672651TC25INTERGENIChomozygous68485056
97067412670674127CT26INTERGENIChomozygous69007678
97067566070675661TC32INTERGENIChomozygous69007681
97067807770678078AG30GENIChomozygous68485060
97067824870678249TC21GENIChomozygous68485063
97067941970679420GC26GENIChomozygous69007684
97068417070684171AG30GENIChomozygous68485066
97068463770684638AT21GENIChomozygous69007687
97068649870686499TA45GENICpossibly homozygous68485072
97067237270672373AG7INTERGENICpossibly homozygous69215930
97067673470676735TC53INTERGENIChomozygous69215931
97067675870676759GC60GENIChomozygous69215932