chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17819039578190395G29GENICpossibly homozygous127396723
17819039678190397T30GENICheterozygous127396724
17819042078190420T35GENIChomozygous127396725
17819075478190755C34GENIChomozygous127396726
17819078878190788G31GENIChomozygous127396727
17819079278190793C29GENIChomozygous127396728
17819082778190828AG21GENIChomozygous120472112
17819082878190829GA20GENIChomozygous120481016
17819084778190848C18GENIChomozygous127396729
17819086578190865T12GENIChomozygous127396730
17819087378190874CT8GENIChomozygous108728718
17819087578190876T8GENIChomozygous127396731
17819287178192873AC37GENIChomozygous127396732
17819292178192922C39GENIChomozygous127396733
17819293578192935A45GENIChomozygous127396734
17819294878192949A46GENIChomozygous127396735
17819296078192961G47GENIChomozygous127396736
17819296778192968G47GENIChomozygous127396737
17819298278192984GC43GENIChomozygous127396738
17819299978193000T41GENIChomozygous127396739
17819301878193019C40GENIChomozygous127396740
17819302078193021T41GENIChomozygous127396741