chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2250997221250997222GT34GENIChomozygous110382243
2250998053250998054AG30GENIChomozygous110382245
2250998627250998628CT16GENIChomozygous111035748
2250998847250998848CT27GENIChomozygous110382251
2250999575250999576CA25GENIChomozygous111035750
2251000529251000530GA23GENIChomozygous110382253
2251000718251000719AT11GENIChomozygous110382254
2251000803251000804CT19GENIChomozygous110852151
2251000849251000850AC25GENIChomozygous110852153
2251000926251000927GA17GENIChomozygous110852155
2251002391251002392CT20GENIChomozygous111035754
2251003077251003078GT18GENIChomozygous111035756
2251003812251003813GA28GENIChomozygous111035758
2251006287251006288TC25GENIChomozygous110382266
2251009440251009441AG28GENIChomozygous110382286
2251010573251010574TG25GENIChomozygous110852179
2251012813251012814CA39GENIChomozygous111035762
2251012927251012928GA31GENIChomozygous111035764
2251016964251016965AG32GENIChomozygous110382322
2251018523251018524TG12GENICpossibly homozygous110382328
2251020803251020804TA35GENIChomozygous110852204
2251021160251021161CT31GENIChomozygous111035786
2251021161251021162AG30GENIChomozygous110382332
2251021166251021167AG29GENIChomozygous110382334
2251021715251021716GA23GENIChomozygous111035788
2251022350251022351TC16GENIChomozygous110382336
2251023206251023207AG12GENIChomozygous110382338
2251024130251024131AG31GENIChomozygous110382340
2251024632251024633CT21GENIChomozygous110382342
2251029266251029267AG19GENIChomozygous110382354
2251030849251030850AG28GENIChomozygous110382360
2251031299251031300TC16GENIChomozygous110382366