chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173567868735678688GC68GENIChomozygous111034863
173567904935679050GT61GENICpossibly homozygous111034865
173567948035679481TC58GENIChomozygous111196616
173567954135679542CT64GENIChomozygous111034867
173567977735679778AT51GENICpossibly homozygous111034869
173568063135680632AG79GENIChomozygous111034871
173568114935681150CT79GENIChomozygous111034873
173568138735681388TG49GENIChomozygous111034875
173568203235682033GA56GENIChomozygous111034877
173568221335682214GA46GENIChomozygous111034879