chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71125439011254391CT13GENIChomozygous53787853
71125452611254527GT16GENICpossibly homozygous53787855
71125474711254748CT14GENIChomozygous53787856
71125478611254787TC3GENIChomozygous53787858
71125480211254803AC8GENICpossibly homozygous53787860
71125511711255118TC8GENIChomozygous53787861
71125557211255573CT19GENICpossibly homozygous53787863
71125754711257548TC10GENIChomozygous53787864
71125768411257685CA20GENICpossibly homozygous53787866
71125777511257776TTTGAA4GENICheterozygous53787868
71125795511257956TC6GENIChomozygous53787869
71125796711257968GA4GENIChomozygous53787871
71125822811258229AG20GENICpossibly homozygous53787872
71125841011258411CT9GENICpossibly homozygous53787874
71125872211258723TC25GENICpossibly homozygous53787875