chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86039337860393379TG27GENIChomozygous53273089
86039338060393381CT28GENIChomozygous53700822
86039434560394346AT22GENIChomozygous53273092
86039442560394426CT21GENIChomozygous53273093
86039465260394653TC20GENIChomozygous52984379
86039473560394736AATGTGTG7GENICpossibly homozygous53388859
86039473560394736AATGTGTGTG7GENICheterozygous53550763
86039496560394969TTTT----27GENIChomozygous53700823
86039497460394975G-24GENIChomozygous53700824
86039597160395972CG24GENIChomozygous53300370
86039606560396068CCC---5GENICheterozygous53273097
86039627760396278CG18GENIChomozygous53300371
86039656860396569AG25GENIChomozygous53300372
86039661160396612GA22GENIChomozygous53273098
86039708560397086AC48GENIChomozygous53273099
86039783660397838TT--7GENICheterozygous53300373
86039806960398070AC25GENIChomozygous52984381
86039856660398567AT23GENIChomozygous53614946
86039882260398823CT36GENIChomozygous52984382
86039887060398871G-18GENIChomozygous52984383
86039961560399616TG30GENIChomozygous53273102
86039973860399739AATTT11GENICpossibly homozygous53300374
86040073060400731AT26GENIChomozygous53273105
86040103960401040TA19GENIChomozygous53273106
86039783760397838T-7GENICheterozygous52666440