chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1109075741109075742TA12GENIChomozygous108174236
1109076634109076635GT13GENIChomozygous108174237
1109084785109084786CA19GENIChomozygous108174245
1109079589109079590TG21GENIChomozygous108174241
1109080239109080240TA17GENIChomozygous108174242
1109082572109082573CA23GENIChomozygous108174243
1109084373109084374GA21GENIChomozygous108174244
1109085756109085757CT9GENIChomozygous108174246
1109085826109085827GC17GENIChomozygous108174247
1109085833109085834CT17GENIChomozygous108174248
1109086121109086122TC17GENIChomozygous108174249
1109086562109086563TA23GENIChomozygous108174250
1109086825109086826TC25GENIChomozygous108174251
1109087540109087541TC21GENIChomozygous108174254
1109087773109087774GA29GENIChomozygous108174255
1109087957109087958TC19GENICpossibly homozygous108174256
1109088046109088047GC21GENIChomozygous108174257
1109088097109088098GC20GENICpossibly homozygous108174258
1109088167109088168GT19GENICpossibly homozygous108174259
1109088259109088260CT19GENIChomozygous108174260
1109088597109088598TC24GENIChomozygous108174263
1109088827109088828AT20GENIChomozygous108174264
1109089113109089114CT22GENIChomozygous108174265
1109089217109089218TC18GENIChomozygous108174266
1109089409109089410CG21GENIChomozygous108174267
1109089443109089444GA18GENIChomozygous108174268
1109089800109089801CT31GENIChomozygous108174269
1109090103109090104TC8GENIChomozygous108174274
1109090180109090181GT10GENIChomozygous108174276
1109090223109090224CT9GENIChomozygous108174277
1109090268109090269TC12GENIChomozygous108174278
1109090411109090412GC14GENIChomozygous108174279
1109091190109091191GA22GENIChomozygous108174280
1109091619109091620AT22GENIChomozygous108174281
1109091803109091804AC20GENIChomozygous108174282
1109092474109092475CT26GENIChomozygous108174283
1109092737109092738AG34GENIChomozygous108174284
1109090101109090102TC7GENIChomozygous120669355