chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1109075741109075742TA18GENIChomozygous108174236
1109076634109076635GT17GENIChomozygous108174237
1109078281109078282TG20GENIChomozygous108174239
1109079589109079590TG27GENIChomozygous108174241
1109080239109080240TA19GENIChomozygous108174242
1109082572109082573CA25GENIChomozygous108174243
1109084373109084374GA20GENIChomozygous108174244
1109084785109084786CA21GENIChomozygous108174245
1109085756109085757CT11GENIChomozygous108174246
1109085826109085827GC12GENIChomozygous108174247
1109085833109085834CT11GENIChomozygous108174248
1109086121109086122TC33GENIChomozygous108174249
1109086562109086563TA22GENIChomozygous108174250
1109086825109086826TC16GENIChomozygous108174251
1109087445109087446GT14GENIChomozygous108174253
1109087540109087541TC19GENIChomozygous108174254
1109087773109087774GA34GENICpossibly homozygous108174255
1109087957109087958TC32GENICpossibly homozygous108174256
1109088046109088047GC25GENICpossibly homozygous108174257
1109088097109088098GC19GENICpossibly homozygous108174258
1109088167109088168GT22GENIChomozygous108174259
1109088259109088260CT21GENIChomozygous108174260
1109088597109088598TC22GENIChomozygous108174263
1109088827109088828AT33GENIChomozygous108174264
1109089443109089444GA19GENIChomozygous108174268
1109089113109089114CT30GENIChomozygous108174265
1109089217109089218TC23GENIChomozygous108174266
1109089409109089410CG26GENIChomozygous108174267
1109089800109089801CT23GENIChomozygous108174269
1109090180109090181GT19GENIChomozygous108174276
1109090223109090224CT15GENIChomozygous108174277
1109090268109090269TC21GENIChomozygous108174278
1109090411109090412GC32GENIChomozygous108174279
1109091190109091191GA17GENIChomozygous108174280
1109091619109091620AT26GENIChomozygous108174281
1109091803109091804AC36GENIChomozygous108174282
1109092474109092475CT36GENIChomozygous108174283
1109092737109092738AG39GENIChomozygous108174284