chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8121844635121844636TC22GENIChomozygous610826505
8121845538121845539AAACACACACACACAC6GENIChomozygous735759224
8121845622121845623TC13GENIChomozygous610826506
8121845798121845799GC12GENIChomozygous610826507
8121847010121847011AG27GENIChomozygous610826508
8121847014121847015CT24GENIChomozygous610826509
8121847292121847293AAC27GENICpossibly homozygous735759225
8121847294121847295AAAC25GENIChomozygous735759226
8121847499121847500GGAC12GENICpossibly homozygous735759227
8121848033121848043AAAAAAAAAA----------6GENICheterozygous735759228
8121848289121848290GGA13GENICheterozygous735759229