chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227070573227070584CTGCTCTCGTG37GENIChomozygous135463368
1227070881227070882AC42GENIChomozygous135822641
1227070883227070883TTCA43GENIChomozygous135463369
1227071750227071751GA35GENICpossibly homozygous135822642
1227072094227072095T30GENICpossibly homozygous135463370