chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122202793222027933CA30GENIChomozygous142323351
122202818722028188GA32GENIChomozygous142323352
122202823522028236GT31GENIChomozygous142323353
122202826422028265TC34GENIChomozygous142323354
122202827722028278CT36GENIChomozygous142323355
122202906922029070CT37GENIChomozygous139110294
122203047422030475AG30GENIChomozygous139110295
122203318922033190TC34GENIChomozygous139110300
122203336222033363GA21GENIChomozygous142323356
122203414822034149AG28GENIChomozygous139110303
122203423122034232AG35GENIChomozygous139110304
122203456222034563GA24GENIChomozygous142323357
122203522222035223AG38GENIChomozygous139110305
122203575222035753CT33GENIChomozygous142323358
122203834722038348TC28GENIChomozygous142323359
122203837822038378G36GENIChomozygous139047017
122203848322038484GT40GENIChomozygous139110312
122203856222038562TCGTGAGCGAG29GENIChomozygous139047018
122203859422038595AG26GENIChomozygous139110313
122203956022039561GA32GENIChomozygous142323360
122204007622040077C29GENIChomozygous139047020
122204034022040340A18GENIChomozygous139047021
122204034122040341GCTGTGCATGGAAAAA18GENIChomozygous139047022
122204055522040556CT41GENIChomozygous142323361
122204056522040566GC39GENIChomozygous142323362
122203626322036264G40GENIChomozygous142310304
122204087922040880CT31GENIChomozygous142323363
122204131222041313GA27GENIChomozygous142323364
122204169622041697CT18GENIChomozygous142323365
122204183222041833AG18GENIChomozygous142323366
122204438422044385CA47GENIChomozygous142323367
122204696422046965AG28GENIChomozygous139110325
122204919122049192TC13GENIChomozygous139110334
122205164122051647GTTGTC34GENIChomozygous142310305
122205166922051670GA31GENIChomozygous142323368
122205227322052274GA24GENIChomozygous142323369
122205469622054696CA35GENICpossibly homozygous142310306
122205551222055513GC12GENIChomozygous139110352
122205587922055880CA26GENIChomozygous139110354
122205655422056555CT18GENIChomozygous139110356