chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108096952108096953CT63GENIChomozygous117071485
10108098094108098136GGGGTGGTATGTGTGAGTGTATAAGTATGTGTGAAAGTGTGT29GENIChomozygous131711060
10108098215108098215GA26GENIChomozygous131099301
10108098361108098362AG37GENICpossibly homozygous117035255
10108098578108098579AT43GENIChomozygous117035257
10108098623108098624TC42GENIChomozygous117071487
10108098810108098811GA34GENIChomozygous117071489
10108098811108098812CA35GENIChomozygous117071491
10108098846108098847GA31GENIChomozygous117071493
10108098873108098877ATCC26GENIChomozygous133005971
10108098887108098888TC26GENIChomozygous117071495
10108098899108098900C25GENIChomozygous133005972
10108098903108098906CTC24GENIChomozygous133005973
10108098909108098910TC24GENIChomozygous117136330
10108098916108098917CT23GENIChomozygous117136331
10108098945108098946AG28GENIChomozygous117136332