chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101506342415063425CT19GENICpossibly homozygous598234339
101506439215064393CT20GENICpossibly homozygous598234340
101506637815066379CT28GENIChomozygous598234341
101506690815066909GGGAAA15GENIChomozygous726414620
101506756715067568AG16GENICpossibly homozygous598234342
101507089715070915CCTCAAATCCCGCAATGA------------------2GENIChomozygous726414621
101507183015071831AC1GENIChomozygous598234343
101507324615073247GGTCAC4GENIChomozygous726414622
101507474315074744AG18GENIChomozygous598234344
101507677415076775CG11GENICpossibly homozygous596468617
101507824215078243CT20GENICpossibly homozygous598234345
101508039515080396AT2GENIChomozygous598234346
101508051615080517A-14GENICpossibly homozygous726414623
101508177215081773CCT9GENICpossibly homozygous726414624
101508305415083055A-3GENIChomozygous726414625
101508306615083067AT2GENIChomozygous598234347
101508413315084134T-10GENIChomozygous726414626
101508436315084364TC17GENICpossibly homozygous598234348
101508680115086816AACAACAACAACAAC---------------1GENIChomozygous726414627
101508738815087389CG10GENIChomozygous598234349
101508791815087919GT19GENIChomozygous598234350
101508855615088557TC14GENIChomozygous598234351
101508868415088685GA29GENICpossibly homozygous598234352
101508953415089535TC21GENIChomozygous598234353
101509069415090695CCA11GENICheterozygous726414632
101509069515090697AA--11GENICpossibly homozygous726414631
101509078015090781CA15GENIChomozygous598234354
101509177415091775AAAC16GENIChomozygous726414633
101509256015092561CT11GENICpossibly homozygous598234355
101509279015092791GA21GENICpossibly homozygous598234356
101509456615094567GA31GENICpossibly homozygous598234357
101509540315095404AAT3GENICheterozygous726414635