chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151933635719336358AC32GENIChomozygous112662207
151933685419336855GA20GENIChomozygous112465830
151933694519336946TC23GENIChomozygous112465832
151933710419337105CT27GENIChomozygous112465834
151933710919337110GA27GENIChomozygous112465836
151933717019337171GA27GENIChomozygous112465838
151933720119337202AG29GENIChomozygous112465840
151933797319337974CG14GENIChomozygous112465842
151933806519338066GT16GENIChomozygous112465844
151933806619338067AC17GENIChomozygous112465846
151933808719338088GA12GENIChomozygous112465848
151933810119338102GA13GENIChomozygous112465850
151933902519339026CT23GENIChomozygous112662209
151933982319339824TG25GENIChomozygous112465852
151934083619340837AC8GENIChomozygous112465856
151934136019341361TC26GENIChomozygous112465858
151934193819341939GA27GENIChomozygous112465860
151934374319343744GA24GENIChomozygous112662211
151934540619345407TC27GENIChomozygous112465864
151934639719346398CT27GENIChomozygous112465868
151934643619346437CT25GENIChomozygous112465870
151934649719346498TC20GENIChomozygous112465872
151934693319346934GA42GENIChomozygous112465874
151934754719347548CA23GENIChomozygous112465882
151934790019347901TC28GENIChomozygous112465886
151934801319348014GA27GENIChomozygous112465888
151934801519348016GA26GENIChomozygous112465890
151934836219348363AG27GENIChomozygous112465894
151934839319348394CT31GENIChomozygous112662213
151934847419348475TC30GENIChomozygous112465898