chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71125439011254391CT30GENIChomozygous53787853
71125452611254527GT18GENICpossibly homozygous53787855
71125474711254748CT22GENICpossibly homozygous53787856
71125478611254787TC17GENICpossibly homozygous53787858
71125480211254803AC21GENICpossibly homozygous53787860
71125511711255118TC9GENIChomozygous53787861
71125557211255573CT16GENIChomozygous53787863
71125754711257548TC14GENICpossibly homozygous53787864
71125768411257685CA30GENICpossibly homozygous53787866
71125777511257776TTTGAA7GENICpossibly homozygous53787868
71125795511257956TC16GENIChomozygous53787869
71125796711257968GA17GENIChomozygous53787871
71125822811258229AG24GENICpossibly homozygous53787872
71125841011258411CT21GENICpossibly homozygous53787874
71125872211258723TC25GENICpossibly homozygous53787875