chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153355747633557476AGCT51GENIChomozygous131159368
153355756733557568GT56GENICpossibly homozygous112807287
153355756733557567A54GENIChomozygous131159369
153355759533557596CT52GENIChomozygous112807289
153355815633558157GA48GENIChomozygous112807291
153355825033558251AG49GENIChomozygous112807293
153355873933558740TG52GENIChomozygous112807295
153355875033558751AG47GENICpossibly homozygous112807297
153355887733558878CG50GENIChomozygous112807299
153356008133560081T32GENICpossibly homozygous131159370
153355788333557884GA28GENIChomozygous112879084