chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84450310144503102CT10GENIChomozygous645352849
84450321244503213TTA16GENIChomozygous754281340
84450324744503248TC24GENIChomozygous645352850
84450410344504104GC30GENIChomozygous645352851
84450420944504210A-33GENIChomozygous754281341
84450467444504675TC18GENIChomozygous645352852
84450507244505073GGAC18GENICpossibly homozygous754281342
84450510644505107TC18GENICpossibly homozygous645352853
84450530544505306AG19GENICpossibly homozygous645352854
84450532744505328GA13GENIChomozygous645352855
84450568244505683AG27GENIChomozygous645352856
84450637644506377CT21GENIChomozygous645352857
84450663044506631GA31GENICpossibly homozygous645352858
84450704644507055ATAACGACG---------15GENIChomozygous754281343
84450710644507107TC17GENICpossibly homozygous645352859
84450748844507489TC24GENIChomozygous645352860
84450769844507699GA27GENIChomozygous645352861
84450792544507926TC27GENIChomozygous645352862
84450956044509561GA37GENIChomozygous645352863
84450992644509927GC30GENIChomozygous645352864
84451006244510063GA20GENIChomozygous645352865
84451081044510811CA26GENIChomozygous645352866
84451093644510937GGA23GENIChomozygous754281344
84451150244511503TC23GENIChomozygous645352867
84451173744511738AG24GENIChomozygous645352868
84451186844511869TA28GENIChomozygous645352869
84451197444511975GT28GENIChomozygous645352870
84451206744512068AC21GENIChomozygous645352871
84451224844512252ACAC----5GENICheterozygous754281345
84451225044512252AC--5GENICheterozygous754281346
84451268544512686AAC23GENIChomozygous754281349
84451328644513287AC22GENIChomozygous645352872
84451363044513631TA24GENIChomozygous645352873
84451435244514353AG22GENICpossibly homozygous645352874
84451460544514606CT27GENIChomozygous645352875
84451504244515043TC19GENIChomozygous645352876
84451512844515129GA22GENIChomozygous645352877
84451540144515402CT11GENIChomozygous645352878
84451572844515729CCTGCTTGCTAGGCAAG10GENIChomozygous754281350
84451653744516538AT26GENIChomozygous645352879