chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2051247735124774GA21GENICpossibly homozygous885273893
2051264295126430CA26GENIChomozygous885273892
2051270395127040AT24GENIChomozygous885273891
2051271355127136AC8GENICheterozygous885273890
2051271695127170TC4GENIChomozygous885273889
2051274085127409AG20GENICpossibly homozygous885273888
2051276295127630AG8GENIChomozygous885273887
2051280225128023CT15GENIChomozygous885273886
2051283815128382AG22GENIChomozygous885273885
2051284075128408CG9GENIChomozygous885273884
2051294635129464CG9GENIChomozygous885273883
2051300015130002AC15GENIChomozygous885273882
2051300365130037CT22GENIChomozygous885273881
2051348285134829GA7GENIChomozygous885273880
2051365415136542CT12GENIChomozygous885273879
2051372975137298TC26GENIChomozygous885273878