chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84450310144503102CT25GENIChomozygous656760908
84450321244503213TTA18GENIChomozygous761076967
84450324744503248TC21GENICpossibly homozygous656760909
84450410344504104GC31GENIChomozygous656760910
84450420944504210A-23GENIChomozygous761076968
84450467444504675TC25GENICpossibly homozygous656760911
84450507244505073GGAC28GENIChomozygous761076969
84450510644505107TC21GENIChomozygous656760912
84450530544505306AG27GENIChomozygous656760913
84450532744505328GA28GENIChomozygous656760914
84450568244505683AG26GENIChomozygous656760915
84450637644506377CT26GENIChomozygous656760916
84450663044506631GA18GENIChomozygous656760917
84450704644507055ATAACGACG---------25GENIChomozygous761076970
84450710644507107TC31GENIChomozygous656760918
84450748844507489TC26GENIChomozygous656760919
84450769844507699GA20GENICpossibly homozygous656760920
84450792544507926TC24GENIChomozygous656760921
84450956044509561GA31GENIChomozygous656760922
84450992644509927GC29GENIChomozygous656760923
84451006244510063GA31GENIChomozygous656760924
84451081044510811CA21GENIChomozygous656760925
84451093644510937GGA19GENIChomozygous761076971
84451150244511503TC38GENIChomozygous656760926
84451173744511738AG41GENIChomozygous656760927
84451186844511869TA36GENIChomozygous656760928
84451197444511975GT21GENICpossibly homozygous656760929
84451206744512068AC22GENIChomozygous656760930
84451225044512252AC--4GENIChomozygous761076973
84451268544512686AAC35GENIChomozygous761076976
84451328644513287AC26GENIChomozygous656760931
84451363044513631TA18GENIChomozygous656760932
84451435244514353AG26GENIChomozygous656760933
84451460544514606CT37GENICpossibly homozygous656760934
84451504244515043TC23GENIChomozygous656760935
84451512844515129GA23GENIChomozygous656760936
84451540144515402CT12GENIChomozygous656760937
84451572844515729CCTGCTTGCTAGGCAAG5GENIChomozygous761076977
84451653744516538AT21GENIChomozygous656760938