chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5177135512177135513A-28GENIChomozygous56102494
5177137005177137011TGTATG------15GENICpossibly homozygous56102496
5177139561177139562GT16GENIChomozygous56102498
5177139562177139563CT16GENIChomozygous56102500
5177141767177141768GC29GENICheterozygous55850346
5177141768177141769AAG26GENICheterozygous55850347
5177141779177141780AG26GENICheterozygous55850348
5177144464177144465A-1GENIChomozygous55850351
5177145801177145802TA21GENIChomozygous56102502