chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109234226109234227AG50GENIChomozygous51598886
10109234702109234709GCACTAC-------14GENIChomozygous51773530
10109236132109236133TC59GENIChomozygous51598891
10109237695109237696AT13GENICheterozygous51773532
10109238836109238837GC66GENIChomozygous51773534
10109245783109245784TC39GENIChomozygous51598934
10109247074109247075AG75GENIChomozygous51598937
10109247683109247684AG72GENICpossibly homozygous51598942
10109248500109248501CCT16GENIChomozygous51773536