chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71125439011254391CT21GENIChomozygous53787853
71125452611254527GT12GENICheterozygous53787855
71125474711254748CT12GENICpossibly homozygous53787856
71125478611254787TC4GENICheterozygous53787858
71125480211254803AC6GENIChomozygous53787860
71125511711255118TC2GENIChomozygous53787861
71125557211255573CT14GENICpossibly homozygous53787863
71125754711257548TC8GENICpossibly homozygous53787864
71125768411257685CA15GENIChomozygous53787866
71125777511257776TTTGAA6GENICheterozygous53787868
71125795511257956TC1GENIChomozygous53787869
71125796711257968GA6GENIChomozygous53787871
71125822811258229AG20GENICpossibly homozygous53787872
71125841011258411CT5GENICheterozygous53787874
71125872211258723TC17GENIChomozygous53787875