chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104769210847692109TC11GENIChomozygous116931943
104769418747694188CT22GENIChomozygous116587607
104769361747693618GA23GENIChomozygous116587603
104769388847693889CG22GENIChomozygous116587605
104769317747693178CT20GENIChomozygous117059079
104769428847694289CT36GENIChomozygous116587609
104769485647694857CT28GENIChomozygous116587611
104769575547695756GA30GENIChomozygous116587615
104769585347695854CT31GENIChomozygous116587617
104769611747696118TA24GENIChomozygous116587621
104769625947696260TC19GENIChomozygous116587623
104769666547696666GA23GENIChomozygous116587625
104769731647697317AG39GENIChomozygous116587627
104769764947697650CT30GENIChomozygous116587629