chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186191566961915670GT49GENIChomozygous140337422
186191577561915776GA51GENICpossibly homozygous140337423
186191770161917702GC50GENIChomozygous140337424
186191978261919783CA52GENIChomozygous140337425
186191985261919853CT56GENIChomozygous140337426