chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4127561470127561471GA19GENIChomozygous113156932
4127561627127561628GT21GENIChomozygous113156933
4127562140127562141AT17GENICpossibly homozygous113156934
4127562516127562517GA28GENIChomozygous113156935
4127562757127562758TC26GENIChomozygous113156937