chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8121844635121844636TC39GENICpossibly homozygous656879906
8121845282121845283CA7GENIChomozygous656879907
8121845538121845539AAACACACACACACAC2GENIChomozygous761153374
8121845622121845623TC15GENIChomozygous656879908
8121845798121845799GC19GENIChomozygous656879909
8121847010121847011AG29GENICpossibly homozygous656879910
8121847014121847015CT29GENICpossibly homozygous656879911
8121847292121847293AAC17GENIChomozygous761153375
8121847294121847295AAAC18GENIChomozygous761153376
8121847499121847500GGAC17GENIChomozygous761153377
8121848033121848043AAAAAAAAAA----------8GENICheterozygous761153378
8121848289121848290GGA28GENICpossibly homozygous761153379