chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31063503510635036TC35GENIChomozygous111445105
31063576710635768TG41GENIChomozygous111445107
31064184410641845GA33GENIChomozygous111445127
31064213010642131CT29GENIChomozygous112065592
31064429510644296CT22GENIChomozygous112065594
31064624110646242CA31GENIChomozygous112065596
31065643810656439CG23GENIChomozygous111445193
31065703710657038GA35GENIChomozygous112065598
31066853610668537CT17GENIChomozygous112065600
31067033310670334GA51GENIChomozygous112065602
31067085810670859CT23GENIChomozygous112065604
31068002910680030TC28GENIChomozygous111445279
31068837810688379CT17GENIChomozygous111445295
31068984510689846AT28GENIChomozygous111445299
31069120810691209AG7GENIChomozygous119863270
31069192310691924AG5GENIChomozygous111874887
31069209510692096TA21GENIChomozygous111445303
31069210910692110AG21GENIChomozygous111445305
31069356910693570CT25GENIChomozygous111445309
31069423410694235GA18GENIChomozygous111445311