chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101657514416575145TC53GENIChomozygous523731111
101657532216575331GTCCTTCCA---------9GENIChomozygous691074225
101657540116575402AATT21GENICpossibly homozygous691074226
101657561316575614AC22GENIChomozygous521013202
101657571616575717TTA28GENIChomozygous691074227
101657584716575848AG17GENICpossibly homozygous521013203
101657585816575859CT19GENICheterozygous523731112
101657587316575874AG20GENICheterozygous521013204
101657591016575911CT35GENIChomozygous521013205
101657602716576028A-47GENIChomozygous691074228
101657628116576282GA18GENICheterozygous523731113
101657653716576538GGT21GENIChomozygous691074229