chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37992164779921648AG15GENIChomozygous111634801
37992282179922822GA25GENIChomozygous119977080
37992574679925747GA19GENIChomozygous119977081
37992612579926126AG12GENIChomozygous111634803
37992680179926802AC18GENIChomozygous119676834
37992798979927990AG19GENIChomozygous111634804
37992806679928067TA26GENIChomozygous111634805
37992809679928097AG15GENICpossibly homozygous112132952
37992860179928602TC10GENIChomozygous111634806
37992903179929032AG21GENIChomozygous111634808
37992938179929382CG20GENIChomozygous111634809
37992958479929585AG17GENIChomozygous111634811
37992958779929588CT18GENIChomozygous111634812
37992993779929938AG24GENIChomozygous111634814
37993064779930648AG18GENIChomozygous111634815
37993074779930748CT20GENIChomozygous111949807
37993222879932229CT20GENIChomozygous111634816
37993253979932540GC24GENIChomozygous111634817
37993438679934387CT21GENIChomozygous111949809
37993469579934696TG15GENIChomozygous111634818
37993490779934908GA18GENIChomozygous111634819
37993529579935296CT11GENIChomozygous111949811
37993580179935802GA17GENIChomozygous111949813
37993586179935862CT21GENIChomozygous111634820
37993586679935867CG21GENIChomozygous111634821
37993606579936066AG15GENIChomozygous111634822
37993659379936594AG18GENIChomozygous111634823
37993673379936734TC23GENIChomozygous111634824
37993690079936901AG21GENIChomozygous111634825