chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151933637419336375GA22GENIChomozygous112843633
151933902519339026CT10GENIChomozygous112662209
151933982319339824TG13GENIChomozygous112465852
151934078819340789GA5GENICheterozygous112465854
151934083619340837AC3GENIChomozygous112465856
151934136019341361TC8GENIChomozygous112465858
151934193819341939GA9GENIChomozygous112465860
151934374319343744GA16GENIChomozygous112662211
151934522519345226GA9GENIChomozygous112465862
151934540619345407TC14GENIChomozygous112465864
151934546319345464GA11GENIChomozygous112465866
151934639719346398CT14GENIChomozygous112465868
151934643619346437CT17GENIChomozygous112465870
151934649719346498TC16GENIChomozygous112465872
151934693319346934GA17GENIChomozygous112465874
151934728119347282GA20GENIChomozygous112465876
151934736519347366CT13GENIChomozygous112465878
151934750019347501CT14GENIChomozygous112465880
151934754719347548CA16GENIChomozygous112465882
151934768219347683TG21GENIChomozygous112465884
151934790019347901TC13GENIChomozygous112465886
151934801319348014GA17GENIChomozygous112465888
151934801519348016GA17GENIChomozygous112465890
151934829219348293CT31GENIChomozygous112465892
151934836219348363AG25GENIChomozygous112465894
151934845919348460GA15GENIChomozygous112465896
151934847419348475TC15GENIChomozygous112465898
151934860319348603GT19GENIChomozygous129235222
151934245219342453A10GENIChomozygous129235219
151934474819344749A9GENIChomozygous129235220
151934768519347686G22GENIChomozygous129235221
151934370219343720GATGATGATGATGATGAC17GENIChomozygous131156879
151934887719348878GA21GENIChomozygous112465900
151934967419349674TGATGAC18GENIChomozygous129235223