chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71125439011254391CT25GENIChomozygous53787853
71125452611254527GT16GENIChomozygous53787855
71125478611254787TC25GENIChomozygous53787858
71125511711255118TC13GENIChomozygous53787861
71125631711256318GA14GENIChomozygous54181342
71125634511256346GA19GENICpossibly homozygous54181343
71125723111257232CT20GENIChomozygous54181344
71125754711257548TC16GENIChomozygous53787864
71125768411257685CA15GENIChomozygous53787866
71125777511257776TTTGAA12GENIChomozygous53787868
71125790211257903TC10GENIChomozygous54181345
71125822811258229AG20GENIChomozygous53787872
71125841011258411CT14GENIChomozygous53787874
71125845511258456CT13GENIChomozygous54181346
71125872211258723TC13GENIChomozygous53787875
71125909111259092CT27INTERGENIChomozygous54181347