chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3153102863153102864CA24GENIChomozygous112042585
3153104481153104482AG31GENIChomozygous112042586
3153105995153105996CA30GENIChomozygous112042591
3153106414153106415GA17GENIChomozygous112042592
3153106611153106612AG27GENIChomozygous112042593
3153106651153106652TG27GENIChomozygous112042594
3153106715153106716CT16GENIChomozygous112042595
3153106870153106871AC29GENIChomozygous112042596
3153106966153106967AC19GENIChomozygous112042597
3153107297153107298AC24GENIChomozygous112042598
3153108011153108012TC30GENIChomozygous112042600
3153110276153110277CA14GENIChomozygous112042601
3153110645153110646CT23GENIChomozygous112042602
3153110952153110953AG19GENIChomozygous112042603
3153111342153111343AG30GENIChomozygous112042604
3153111884153111885TC20GENIChomozygous112042605
3153111936153111937CT16GENIChomozygous112042606
3153112318153112319CT19GENIChomozygous112042607
3153114684153114685TC12GENIChomozygous112042608