chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102914107929141080G16GENICheterozygous141037065
102914770829147709TA6GENIChomozygous138752259
102921280529212806A6GENICheterozygous403280611
102921280529212806AT6GENICheterozygous403280612
102921280729212808A6GENICheterozygous403280613
102921280729212808AT6GENICheterozygous403280614
102921280929212810A6GENICheterozygous403280615
102921280929212810AT6GENICheterozygous403280616
102921484929214850A21GENICheterozygous138675805
102921484929214850AC21GENICpossibly homozygous403280617
102926551129265512C12GENICheterozygous403280664
102926551129265512CT12GENICheterozygous403280665
102936633929366340TC12GENICheterozygous403280682
102936633929366340T12GENICheterozygous403280683
102938392129383922G14GENICheterozygous403280698
102938392129383922GC14GENICheterozygous403280699
102940083129400832G9GENICheterozygous403280702
102940083129400832GC9GENICheterozygous403280703
102940083629400837AT10GENICheterozygous403280704
102940083629400837A10GENICheterozygous403280705
102943193929431939T19GENIChomozygous138675932
102943946429439464TCCTC4GENIChomozygous144077238