chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142093570320935704CT25GENIChomozygous936199246
142093596520935966GA29GENIChomozygous936199247
142093635020936351GA20GENIChomozygous936199248
142093903820939039AT22GENIChomozygous936199249
142093939420939395AG22GENIChomozygous936199250
142094222920942230TC18GENIChomozygous936199251
142094223220942233CA17GENIChomozygous936199252
142094261420942615GC14GENIChomozygous936199253
142094468420944685AG25GENIChomozygous936199254
142094601420946015AT28GENIChomozygous936199255
142094757020947571AG26GENIChomozygous936199256
142094821820948219GA30GENIChomozygous936199257
142094838320948384GA34GENIChomozygous936199258
142094843520948436AT34GENIChomozygous936199259
142094898520948986GC24GENIChomozygous936199260
142094898920948990TA22GENIChomozygous936199261
142094899220948993GT22GENIChomozygous936199262
142094899820948999TA21GENIChomozygous936199263
142094900620949007AT25GENIChomozygous936199264
142094900820949009GC25GENIChomozygous936199265
142094954020949541TG27GENICpossibly homozygous936199266
142094956220949563AT25GENIChomozygous936199267
142095042120950422CA33GENIChomozygous936199268
142095107520951076CT43GENIChomozygous936199269