chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129798708129798709CT34GENIChomozygous775981166
7129799321129799322GA55GENIChomozygous775981167
7129799658129799659GA47GENIChomozygous775981168
7129800613129800614CT39GENIChomozygous775981169
7129801117129801118AG30GENIChomozygous775981170
7129801936129801937GA24GENIChomozygous775981171
7129803953129803954CG40GENICpossibly homozygous775981172
7129804694129804695TG69GENIChomozygous775981173
7129804776129804777TC47GENIChomozygous775981174
7129804821129804822GA54GENIChomozygous775981175
7129805161129805162TC50GENICpossibly homozygous775981176
7129805282129805283AG48GENIChomozygous775981177
7129805315129805316TC41GENIChomozygous775981178
7129805327129805328GT46GENIChomozygous775981179
7129805454129805455CA44GENIChomozygous775981180
7129805486129805487TC49GENIChomozygous775981181
7129805522129805523TC51GENIChomozygous775981182
7129805543129805544GA46GENIChomozygous775981183
7129806000129806001CT51GENIChomozygous775981184
7129806589129806590CT57GENIChomozygous775981185
7129807333129807334GA47GENIChomozygous775981186
7129807636129807637CA40GENIChomozygous775981187
7129808320129808321TC30GENICheterozygous775981188
7129808777129808778CT56GENIChomozygous775981189
7129808911129808912GT59GENIChomozygous775981190
7129808987129808988AG46GENIChomozygous775981191
7129810320129810321TC34GENIChomozygous775981192
7129810349129810350TC38GENIChomozygous775981193
7129810795129810796CT55GENIChomozygous775981194
7129810829129810830GA53GENIChomozygous775981195
7129811223129811224AG46GENIChomozygous775981196