chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122467780924677810CG24GENIChomozygous642599266
122467825624678257GA16GENIChomozygous642599267
122467838124678382CCA18GENIChomozygous752670580
122467854524678546CCCTAA22GENIChomozygous752670581
122467870324678704TTAGGCTTGTAC26GENIChomozygous752670582
122467977924679780AG27GENIChomozygous642599268
122468020124680202AG20GENIChomozygous642599269
122468023624680237CT23GENIChomozygous642599270
122468114124681142AG29GENIChomozygous642599271
122468196524681981CCTTCCTTCCTTCCTC----------------9GENIChomozygous752670583
122468201324682014CT27GENIChomozygous642599272
122468211024682114CTTT----20GENIChomozygous752670584
122468221524682216CT15GENIChomozygous642599273
122468260324682604GT38GENIChomozygous642599274
122468286724682868AG31GENIChomozygous642599275
122468291924682920CT19GENIChomozygous642599276
122468295524682956GA23GENIChomozygous642599277
122468314724683148CT27GENIChomozygous642599278
122468339724683398C-19GENIChomozygous752670585
122468339924683400CT19GENIChomozygous642599279
122468383124683832AT14GENIChomozygous642599280
122468383424683835GT13GENIChomozygous642599281
122468497724684979TT--11GENIChomozygous752670587
122468810624688107TC22GENIChomozygous642599282
122468818424688185GA25GENIChomozygous642599283
122468822624688227TA27GENIChomozygous642599284