chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151933637419336375GA64GENIChomozygous112843633
151933902519339026CT49GENIChomozygous112662209
151933982319339824TG57GENIChomozygous112465852
151934078819340789GA23GENIChomozygous112465854
151934083619340837AC17GENIChomozygous112465856
151934136019341361TC51GENIChomozygous112465858
151934193819341939GA58GENICpossibly homozygous112465860
151934374319343744GA47GENIChomozygous112662211
151934522519345226GA52GENIChomozygous112465862
151934540619345407TC42GENIChomozygous112465864
151934546319345464GA31GENIChomozygous112465866
151934639719346398CT45GENIChomozygous112465868
151934643619346437CT40GENIChomozygous112465870
151934649719346498TC46GENIChomozygous112465872
151934693319346934GA33GENIChomozygous112465874
151934728119347282GA39GENIChomozygous112465876
151934736519347366CT37GENIChomozygous112465878
151934750019347501CT50GENIChomozygous112465880
151934754719347548CA53GENIChomozygous112465882
151934768219347683TG60GENIChomozygous112465884
151934790019347901TC52GENIChomozygous112465886
151934801319348014GA52GENIChomozygous112465888
151934801519348016GA53GENIChomozygous112465890
151934829219348293CT64GENIChomozygous112465892
151934836219348363AG57GENIChomozygous112465894
151934845919348460GA52GENIChomozygous112465896
151934847419348475TC52GENIChomozygous112465898
151934768519347686G61GENIChomozygous129235221
151934860319348603GT40GENIChomozygous129235222
151934245219342453A38GENICpossibly homozygous129235219
151934474819344749A46GENIChomozygous129235220
151934370219343720GATGATGATGATGATGAC42GENIChomozygous131156879
151934887719348878GA53GENIChomozygous112465900
151934967419349674TGATGAC58GENIChomozygous129235223