chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4175841321175841322T19GENICheterozygous133132898
4175847750175847750T36GENIChomozygous128107358
4175858152175858153C17GENIChomozygous128107365
4175858075175858076T38GENIChomozygous128107362
4175858104175858104T38GENIChomozygous128107363
4175858149175858150G17GENIChomozygous128107364
4175858184175858185G13GENIChomozygous128107366
4175869536175869536TAAAACATGCTTTAAAGTCCTCAGTAAGTGGTATCTTTCCTGCAAGGATTAAGGATCAGTCACATTTCAAGAAAACTGAAGTTCAAAGTGCTAATACATATTGGTTACTCACAAAACACGAGGTTATCTCTTGTCAGGAGAGGTGAAGTGGTTCCTTCCACCTGACTGAAGGACATACCTACTGAGCAATTACACATCAAGTAGT36GENICpossibly homozygous128107373