chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142093570320935704CT15GENIChomozygous800242281
142093596520935966GA21GENIChomozygous800242282
142093635020936351GA23GENIChomozygous800242283
142093783520937836TG15GENICpossibly homozygous800242284
142093833620938337TG45GENIChomozygous800242285
142093903820939039AT29GENIChomozygous800242286
142093939420939395AG27GENIChomozygous800242287
142094164320941644AG31GENICpossibly homozygous800242288
142094166320941664GC26GENIChomozygous800242289
142094170220941703CA14GENIChomozygous800242290
142094170520941706GA14GENIChomozygous800242291
142094203720942038TG8GENICpossibly homozygous800242292
142094208520942086CA16GENIChomozygous800242293
142094214020942141CG11GENIChomozygous800242294
142094222920942230TC22GENIChomozygous800242295
142094223220942233CA21GENIChomozygous800242296
142094261420942615GC29GENIChomozygous800242297
142094468420944685AG12GENIChomozygous800242298
142094491220944913AG26GENIChomozygous800242299
142094601420946015AT25GENIChomozygous800242300
142094757020947571AG23GENIChomozygous800242301
142094821820948219GA15GENIChomozygous800242302
142094838320948384GA22GENIChomozygous800242303
142094843520948436AT29GENIChomozygous800242304
142094898520948986GC27GENIChomozygous800242305
142094899820948999TA31GENIChomozygous800242306
142094900620949007AT33GENIChomozygous800242307
142094900820949009GC33GENIChomozygous800242308
142094954020949541TG27GENIChomozygous800242309
142094956220949563AT27GENIChomozygous800242310
142095042120950422CA25GENIChomozygous800242311
142095107520951076CT18GENIChomozygous800242312
142095222620952227CT39GENIChomozygous800242313