chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5177135512177135513A-20GENICpossibly homozygous56102494
5177137005177137011TGTATG------29GENIChomozygous56102496
5177139561177139562GT34GENIChomozygous56102498
5177139562177139563CT34GENIChomozygous56102500
5177141744177141745TTAGGTGGAGAGGAGAGGAGGCAGC27GENIChomozygous56366154
5177144463177144465AA--14GENICheterozygous55850350
5177144464177144465A-14GENICheterozygous55850351
5177145801177145802TA32GENIChomozygous56102502