chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1168910966168910967TC29GENIChomozygous60937182
1168911846168911847GT35GENIChomozygous60937183
1168912075168912076CG32GENIChomozygous60937184
1168912305168912327CTTCCTTCTTCTTCTTCTTCTT----------------------10GENIChomozygous62369195
1168913770168913771GA39GENIChomozygous60937188
1168915031168915032CT35GENIChomozygous60937189
1168916473168916474AC41GENIChomozygous60937190
1168916569168916570TC48GENIChomozygous60937191
1168916582168916583CT52GENIChomozygous60937192
1168916870168916871AG18GENIChomozygous60937193
1168916881168916882GGTTTGT12GENICpossibly homozygous60937194
1168917084168917085AG24GENIChomozygous60937195
1168917128168917129CT31GENIChomozygous60937196
1168917168168917169GT41GENIChomozygous60937197
1168918752168918753T-10GENIChomozygous60937198
1168918852168918853TG20GENIChomozygous60937199
1168919337168919338TA46GENIChomozygous60937200
1168913472168913478GCACAC------8GENICpossibly homozygous62247702
1168913472168913480GCACACAC--------8GENICheterozygous62247701