chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122447360024473601AACATCGGGACTTTGCATTCTTCTACCCCATGGAAAAGATAGTTTTTTGT19GENIChomozygous752670331
122447384924473850G-13GENIChomozygous752670332
122447401624474017A-10GENIChomozygous752670333
122447438524474386CA17GENIChomozygous642598861
122447452024474521CT16GENIChomozygous642598862
122447803224478033GT26GENIChomozygous642598863
122447971624479717AG16GENIChomozygous642598864
122448460124484602CT16GENIChomozygous642598865
122448471824484722TGTC----26GENICpossibly homozygous752670334