chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71125439011254391CT19GENIChomozygous53787853
71125452611254527GT30GENIChomozygous53787855
71125478611254787TC33GENIChomozygous53787858
71125511711255118TC30GENIChomozygous53787861
71125631711256318GA32GENIChomozygous54181342
71125634511256346GA40GENIChomozygous54181343
71125723111257232CT17GENIChomozygous54181344
71125754711257548TC26GENIChomozygous53787864
71125768411257685CA32GENIChomozygous53787866
71125777511257776TTTGAA32GENIChomozygous53787868
71125790211257903TC32GENIChomozygous54181345
71125822811258229AG28GENICpossibly homozygous53787872
71125841011258411CT26GENIChomozygous53787874
71125845511258456CT26GENIChomozygous54181346
71125872211258723TC30GENIChomozygous53787875
71125909111259092CT29INTERGENIChomozygous54181347