chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1168910966168910967TC14GENIChomozygous60937182
1168911846168911847GT17GENIChomozygous60937183
1168912075168912076CG21GENIChomozygous60937184
1168912309168912322CTTCTTCTTCTTC-------------2GENICheterozygous62313504
1168913472168913478GCACAC------5GENICheterozygous62247702
1168913770168913771GA26GENIChomozygous60937188
1168916473168916474AC20GENIChomozygous60937190
1168916569168916570TC9GENIChomozygous60937191
1168916582168916583CT10GENIChomozygous60937192
1168916870168916871AG24GENIChomozygous60937193
1168916881168916882GGTTTGT17GENICheterozygous60937194
1168917084168917085AG10GENIChomozygous60937195
1168917128168917129CT16GENIChomozygous60937196
1168917168168917169GT21GENIChomozygous60937197
1168918752168918753T-12GENIChomozygous60937198
1168918852168918853TG32GENIChomozygous60937199
1168919337168919338TA20GENIChomozygous60937200