chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5177135511177135512GGA28GENICpossibly homozygous55850341
5177138651177138652CT47GENIChomozygous55850342
5177138690177138691AG24GENIChomozygous55850343
5177140075177140076GA33GENIChomozygous55850344
5177140402177140414TTTTTTTTTTTT------------16GENIChomozygous55850345
5177141744177141745TTAGGTGGAGAGGAGAGGAGGCAGC32GENIChomozygous56366154
5177144462177144465AAA---23GENICpossibly homozygous55949672
5177144463177144465AA--23GENICheterozygous55850350
5177144925177144926AAG28GENIChomozygous55850352