chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152473511924735120GGT2GENICheterozygous49293903
152473512024735123TTT---2GENICheterozygous48479680
152473516024735161CCTTTTTTTCT1GENIChomozygous48479685
152473524024735264TGTGTGTGTGTGTGTGTGTGTGTG------------------------1GENIChomozygous48479687
152473591624735917TC7GENIChomozygous48479691
152473633924736340CT12GENICpossibly homozygous48479693
152473692224736923TC5GENICheterozygous48479695
152474285724742858GA9GENICpossibly homozygous48570920
152474204624742047TC6GENICheterozygous48570918
152474295224742953AT14GENICpossibly homozygous48570926
152474307724743078AT7GENIChomozygous48570928
152474308424743089GGCAA-----7GENIChomozygous48570930
152474469624744697AG13GENIChomozygous48570932
152474472924744730TC10GENICpossibly homozygous48570934
152474481524744816GA17GENIChomozygous48570936
152474483724744838AG14GENIChomozygous48479709
152474545424745455AG4GENIChomozygous48570938
152474564124745642TC4GENIChomozygous48570940
152474569624745697GA10GENIChomozygous48570942
152474572324745724GA6GENICheterozygous48570944
152474623224746233GA9GENIChomozygous48570946
152474627324746274TG15GENIChomozygous48479715
152474649024746491AG8GENIChomozygous48570948
152474677824746779AAT9GENIChomozygous48570950
152474706924747070AC2GENIChomozygous48570952
152474778924747790TC9GENICpossibly homozygous48479717
152474779324747794TC9GENICpossibly homozygous48570954
152474797924747982TTT---2GENIChomozygous48570956
152474798324747984TC3GENIChomozygous49041116
152474803424748036TT--6GENICheterozygous48570958
152474843924748440TC6GENIChomozygous48570962
152474847024748471AC10GENIChomozygous48570964
152474869024748691GA10GENICpossibly homozygous48570966
152474890624748907GA10GENIChomozygous48479727
152474903824749039GC5GENIChomozygous49041120
152474916124749162AG7GENIChomozygous48570968
152474921524749216CG8GENIChomozygous48570970
152474929924749300GA14GENIChomozygous48570972
152474990024749901TC3GENIChomozygous48570974