chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8121844635121844636TC10GENICpossibly homozygous625576824
8121845622121845623TC13GENIChomozygous625576825
8121845798121845799GC5GENIChomozygous625576826
8121847010121847011AG10GENIChomozygous625576827
8121847014121847015CT10GENIChomozygous625576828
8121847292121847293AAC3GENIChomozygous740849653
8121847294121847295AAAC4GENIChomozygous740849654
8121847499121847500GGAC5GENICheterozygous740849655
8121848289121848290GGA3GENICheterozygous740849657