chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101387494113874942GA22GENIChomozygous142218279
101387496413874965TC24GENIChomozygous142218280
101387661013876610T13GENICpossibly homozygous142196873
101387706713877068TC23GENIChomozygous142218281
101387721413877214AT17GENIChomozygous142196874
101387734413877345A16GENICpossibly homozygous142196875
101387763313877634GA23GENIChomozygous142218282
101387787513877876CA26GENIChomozygous142218283
101388033913880340GC22GENIChomozygous142218284
101388221113882212TC30GENIChomozygous142218285
101388412113884121TGTGTGTGTAGTATGTGG19GENIChomozygous142196876
101388675913886760AG18GENIChomozygous142218286
101388794313887947TTTG30GENIChomozygous142196877
101388833513888336GA28GENIChomozygous142218288
101388724213887243TC15GENIChomozygous142218287