chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122467780924677810CG28GENIChomozygous539367324
122467825624678257GA32GENIChomozygous539367325
122467838124678382CCA20GENIChomozygous697781083
122467854524678546CCCTAA22GENIChomozygous697781085
122467870324678704TTAGGCTTGTAC14GENIChomozygous697781086
122467977924679780AG36GENIChomozygous539367326
122468020124680202AG30GENIChomozygous539367327
122468023624680237CT36GENIChomozygous539367328
122468114124681142AG25GENIChomozygous539367329
122468197824681979CCT8GENICheterozygous697781087
122468197824681979CCCT8GENICheterozygous697781088
122468198424681985TTC13GENICheterozygous697781089
122468198824681989TTC14GENICheterozygous697781090
122468201324682014CT21GENIChomozygous539367330
122468211024682114CTTT----29GENIChomozygous697781091
122468221524682216CT40GENIChomozygous539367331
122468260324682604GT37GENIChomozygous539367332
122468286724682868AG24GENIChomozygous539367333
122468291924682920CT38GENIChomozygous539367334
122468295524682956GA36GENIChomozygous539367335
122468314724683148CT38GENIChomozygous539367336
122468339724683398C-25GENIChomozygous697781092
122468383124683832AT11GENIChomozygous540812054
122468383424683835GT11GENIChomozygous540812055
122468810624688107TC19GENIChomozygous539367337
122468818424688185GA27GENIChomozygous539367338
122468822624688227TA27GENIChomozygous539367339