chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2215036358215036359GA8GENICheterozygous59390005
2215036575215036576CT12GENIChomozygous59390006
2215037995215037996CCT6GENICheterozygous59390007
2215038924215038925GA20GENICpossibly homozygous59390008
2215039299215039300CT16GENICpossibly homozygous59390010
2215040337215040345AAAAAAAA--------2GENIChomozygous59390011
2215041735215041736AG25GENIChomozygous59390013
2215042380215042381C-9GENIChomozygous59390014
2215042407215042408CCT9GENIChomozygous59390015
2215042414215042415TC8GENIChomozygous59390016
2215042442215042443G-1GENIChomozygous59390017
2215042460215042461G-4GENIChomozygous59390019
2215042491215042492TC4GENIChomozygous59390020
2215044484215044485GA22GENICpossibly homozygous59390021
2215046102215046103T-3GENIChomozygous59390025
2215047514215047515GA22GENICpossibly homozygous59390027
2215050359215050360CCAAAACTTGAG1GENIChomozygous59390028
2215050555215050556GA21GENICpossibly homozygous59390029
2215051086215051087AC12GENIChomozygous59390030
2215051239215051240GT21GENICpossibly homozygous59390031
2215051320215051321CT11GENIChomozygous59390032
2215051352215051353TC2GENICheterozygous59390034
2215051552215051553CT2GENIChomozygous60587194
2215051557215051559AT--4GENIChomozygous59390049
2215051976215051977GT18GENIChomozygous59390050
2215052220215052221AG18GENIChomozygous59390051
2215052787215052788GA17GENICpossibly homozygous59390052
2215053291215053292TG13GENICheterozygous59390055
2215052835215052836TC18GENICpossibly homozygous59390053
2215053129215053130GA25GENIChomozygous59390054
2215053866215053867AG13GENICheterozygous59390056
2215054239215054240AG14GENIChomozygous59390057
2215055327215055331TTTA----9GENIChomozygous59390058