chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84450310144503102CT25GENIChomozygous557451149
84450321244503213TTA22GENIChomozygous705320393
84450324744503248TC23GENIChomozygous557451150
84450410344504104GC33GENIChomozygous557451151
84450420944504210A-27GENIChomozygous705320394
84450432944504330A-21GENIChomozygous705320395
84450507244505073GGAC21GENIChomozygous705320397
84450510644505107TC16GENIChomozygous557451152
84450512044505121GA13GENIChomozygous558840075
84450530544505306AG21GENIChomozygous557451153
84450531144505312CA20GENIChomozygous558840076
84450532744505328GA24GENIChomozygous557451154
84450792544507926TC10GENIChomozygous557451155
84450956044509561GA34GENIChomozygous557451156
84450957244509573GT35GENIChomozygous558840077
84450988944509890CT20GENIChomozygous557451157
84450992644509927GC18GENIChomozygous557451158
84451006244510063GA19GENIChomozygous557451159
84451081044510811CA27GENIChomozygous557451160
84451093644510937GGA20GENIChomozygous705320398
84451173744511738AG16GENIChomozygous557451161
84451206744512068AC16GENIChomozygous557451162
84451265244512653TC23GENIChomozygous558840078
84451268544512686AAC21GENIChomozygous705320403
84451328644513287AC22GENIChomozygous557451163
84451363044513631TA27GENIChomozygous557451164
84451376644513767CCA15GENICheterozygous705320404
84451376644513767CCAA15GENICpossibly homozygous705320405
84451504244515043TC21GENIChomozygous557451165
84451533644515348TCGTTTTATTTA------------8GENIChomozygous705320406
84451535044515351TG7GENIChomozygous558840079
84451572844515729CCTGCTTGCTAGGCAAG7GENIChomozygous705320407