chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1211249147211249148CA23GENIChomozygous951536116
1211249164211249165AG27GENIChomozygous951536117
1211249514211249515AG33GENICpossibly homozygous951536118
1211249867211249868GA22GENIChomozygous951536119
1211249879211249880GT24GENIChomozygous951536120
1211250193211250194AC25GENIChomozygous951536121
1211250496211250497TC28GENIChomozygous951536122
1211250622211250623CG22GENIChomozygous951536123
1211250700211250701GA25GENIChomozygous951536124
1211252203211252204AG35GENIChomozygous951536125
1211252276211252277CT13GENIChomozygous951536126
1211252677211252678CT30GENIChomozygous951536127
1211254276211254277AC22GENIChomozygous951536128
1211254477211254478TC10GENIChomozygous951536129
1211254496211254497CT10GENIChomozygous951536130
1211255440211255441GT39GENIChomozygous951536131
1211255616211255617AT29GENIChomozygous951536132
1211256722211256723TC29GENIChomozygous951536133
1211257074211257075AG37GENIChomozygous951536134
1211258234211258235GA37GENIChomozygous951536135
1211258541211258542CT31GENIChomozygous951536136
1211258803211258804TC31GENIChomozygous951536137
1211259421211259422AG12GENIChomozygous951536138
1211259737211259738AG26GENIChomozygous951536139
1211259868211259869CT19GENIChomozygous951536140
1211261011211261012GA35GENIChomozygous951536141
1211261278211261279AG34GENIChomozygous951536142
1211261430211261431CT35GENIChomozygous951536143
1211261727211261728CT21GENIChomozygous951536144
1211262253211262254CT34GENIChomozygous951536145
1211262513211262514GA34GENIChomozygous951536146
1211262865211262866AG19GENIChomozygous951536147
1211263517211263518CA29GENIChomozygous951536148
1211264098211264099TG16GENIChomozygous951536149
1211264888211264889CA19GENIChomozygous951536150
1211264889211264890TA19GENIChomozygous951536151