chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8121844635121844636TC17GENIChomozygous638323876
8121845538121845539AAACACACACACACAC16GENIChomozygous749921899
8121845622121845623TC18GENIChomozygous638323877
8121845798121845799GC28GENIChomozygous638323878
8121847010121847011AG30GENIChomozygous638323879
8121847014121847015CT30GENIChomozygous638323880
8121847292121847293AAC24GENIChomozygous749921900
8121847294121847295AAAC23GENIChomozygous749921901
8121847499121847500GGAC17GENIChomozygous749921902
8121848033121848043AAAAAAAAAA----------13GENICheterozygous749921903
8121848289121848290GGA32GENICpossibly homozygous749921904