chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2174064050174064051TA36GENIChomozygous120128971
2174070138174070139CT23GENIChomozygous110135086
2174070173174070174CT19GENIChomozygous110135087
2174070176174070177CA19GENIChomozygous110612143
2174070177174070178CA19GENIChomozygous110612144
2174070178174070179CT18GENIChomozygous110612145
2174070183174070184CT19GENIChomozygous110135088
2174070195174070196CA21GENIChomozygous110135089
2174070199174070200CA24GENIChomozygous110135090
2174070230174070231CA26GENIChomozygous110135091
2174103321174103322AG25GENIChomozygous110902201
2174103424174103425AG23GENIChomozygous110135137
2174104327174104328GA22GENIChomozygous110135138
2174104432174104433GT34GENIChomozygous110135139
2174104507174104508TC21GENIChomozygous110135140
2174104528174104529GA17GENIChomozygous110135141
2174104602174104603AG19GENIChomozygous110135142
2174104644174104645TC20GENIChomozygous110135143
2174105360174105361TA13GENIChomozygous110135146
2174105366174105367CA12GENIChomozygous110135147
2174106107174106108GA11GENIChomozygous110793752
2174106498174106499TA17GENIChomozygous110135148
2174106659174106660CA15GENIChomozygous110135149
2174107054174107055AT20GENIChomozygous110135151
2174107361174107362TC30GENIChomozygous110135153
2174107545174107546TC21GENIChomozygous110135154
2174107740174107741AT17GENIChomozygous110135155
2174108005174108006TC13GENIChomozygous110135156
2174108221174108222AG27GENIChomozygous110135157
2174108659174108660AG20GENIChomozygous110135159
2174108742174108743AC29GENIChomozygous110135160
2174108787174108788TC27GENIChomozygous110135161
2174108996174108997TC23GENIChomozygous110135163
2174109175174109176GC25GENIChomozygous110135164
2174109792174109793TC23GENIChomozygous110135165
2174109977174109978AG23GENIChomozygous111143982
2174110308174110309GA22GENIChomozygous110135166
2174111168174111169GT25GENIChomozygous110135168
2174111353174111354CT29GENIChomozygous110135169
2174111420174111421TC24GENIChomozygous110135170