chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214123032214123033GT2GENIChomozygous108990192
1214123787214123788CT31GENIChomozygous108990193
1214124348214124349AG5GENIChomozygous108532211
1214125087214125088GA21GENIChomozygous108990194
1214126106214126107GA27GENICpossibly homozygous108990195
1214126509214126510CT11GENIChomozygous108990196
1214126604214126605CT3GENIChomozygous108532220
1214130422214130423CA30GENICpossibly homozygous108990197
1214130767214130768AG29GENIChomozygous108990198
1214131357214131358AG30GENIChomozygous108532226
1214131750214131751CT24GENIChomozygous108990199
1214132380214132381AG16GENIChomozygous108532227
1214133078214133079GA31GENIChomozygous108990200
1214134834214134835GA16GENIChomozygous108990201
1214138857214138858GT21GENIChomozygous108990202
1214140127214140128AC22GENIChomozygous108990203
1214140827214140828GT22GENIChomozygous108532233
1214141343214141344AG20GENICpossibly homozygous108532235
1214142748214142749GA18GENIChomozygous108990204
1214146027214146028TC17GENIChomozygous108532239