chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151862649118626492CT17GENIChomozygous112464732
151862749618627497CT20GENIChomozygous112464734
151862754618627547TC20GENICpossibly homozygous112464736
151862765918627660AG14GENIChomozygous112464738
151862777218627773AG22GENIChomozygous112464740
151862818118628182TC27GENIChomozygous112464744
151862821918628220CT29GENIChomozygous112464746
151862894018628941CG19GENIChomozygous112464748
151862963718629638TA21GENIChomozygous113052098
151862999018629991CT19GENIChomozygous112464750
151863494918634950TC26GENIChomozygous112464754
151863524418635245TC27GENIChomozygous112464756
151863253618632537AG20GENIChomozygous112662012
151862964618629647GC19GENIChomozygous113070152