chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71125439011254391CT22GENIChomozygous53787853
71125452611254527GT16GENIChomozygous53787855
71125474711254748CT20GENIChomozygous53787856
71125478611254787TC11GENIChomozygous53787858
71125480211254803AC16GENICpossibly homozygous53787860
71125511711255118TC6GENIChomozygous53787861
71125557211255573CT20GENICpossibly homozygous53787863
71125754711257548TC17GENIChomozygous53787864
71125768411257685CA36GENIChomozygous53787866
71125777511257776TTTGAA6GENIChomozygous53787868
71125795511257956TC7GENICpossibly homozygous53787869
71125796711257968GA11GENIChomozygous53787871
71125822811258229AG20GENICpossibly homozygous53787872
71125841011258411CT11GENIChomozygous53787874
71125872211258723TC18GENIChomozygous53787875