chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51852122318521225GA--7GENIChomozygous56306389
51852346518523466AG9GENIChomozygous55225908
51852370218523703AT8GENIChomozygous56306390
51852511118525112AC8GENIChomozygous55225914
51852513118525132TA12GENIChomozygous55225916
51852659418526595AG18GENIChomozygous55225921
51852661218526613TC16GENIChomozygous56306391
51852855818528559GA13GENIChomozygous56306393
51852876718528768AT22GENIChomozygous56306394
51852891218528913TA19GENIChomozygous56566342
51852966818529669TTGGG15GENIChomozygous55225926
51853007618530086AGAGAGAGAG----------26GENICpossibly homozygous56566343
51853043118530432AG13GENIChomozygous56306397
51853058018530581GA15GENIChomozygous56306398
51853143618531437GC29GENICpossibly homozygous56306399
51853197518531976GA13GENIChomozygous56306400
51853269418532695CT29GENIChomozygous55225935
51853294918532950GGCACACACACA10GENICheterozygous56397564
51853337718533378TTACAC11GENICheterozygous56577753
51853342118533422CCA24GENICheterozygous56566344
51853393418533935TC21GENIChomozygous56306401