chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
728287052828706CT52GENICpossibly homozygous115977159
728292472829251TTAA41GENIChomozygous132980894
728302642830264C53GENIChomozygous132980895
728304242830424ATA42GENIChomozygous128432357
728304902830491GA52GENIChomozygous115977161
728315042831505AG54GENIChomozygous115545942
728326552832656TG47GENIChomozygous115545944
728327102832711GA49GENIChomozygous115977163
728337392833741AC41GENIChomozygous132980896
728340912834092CT39GENIChomozygous115977165
728347492834750GA49GENIChomozygous115977167
728365182836520AC40GENIChomozygous132980897
728368622836863GA46GENICpossibly homozygous115977169
728371542837155AG49GENIChomozygous115977171
728375662837567GA35GENIChomozygous115977173
728391342839135GA45GENIChomozygous115977181
728408522840853TC50GENIChomozygous115545952
728413452841346CT43GENIChomozygous115977183
728414892841490TG43GENIChomozygous115977185
728430722843077TGGGG57GENIChomozygous132980899
728488932848894CT59GENIChomozygous115977197
728430702843071GT57GENIChomozygous115977187
728436052843606AG43GENIChomozygous115545956
728436892843690CT50GENIChomozygous115977189
728479512847952GC44GENIChomozygous115977195
728493072849308AG74GENIChomozygous115545968
728495372849538CT67GENIChomozygous115977199
728499372849938GT46GENIChomozygous115977201
728505292850530GA41GENIChomozygous115977203
728510082851009TC41GENIChomozygous115977205
728520252852026CT61GENIChomozygous115977207
728520512852100GAGTGAGGCATTTCTACACTTGATCTTAGCCAAAAGGCCGAGAAGCGAT43GENIChomozygous131007024
728526542852654A51GENICpossibly homozygous131007026
728534092853410AG67GENIChomozygous115545974
728540832854084GA62GENIChomozygous115977209