chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77051304770513048AG37GENICpossibly homozygous68870406
77051320870513209GC66GENIChomozygous68870408
77051331670513317CA38GENICpossibly homozygous71499048
77051346270513463TC38GENIChomozygous68870410
77051350370513504AT42GENICpossibly homozygous68870412
77051398370513984AG67GENIChomozygous68870414
77051436970514370AG63GENIChomozygous68870416
77051518170515182TC53GENIChomozygous68870418
77051558770515588GA55GENIChomozygous68870420
77051580370515804AG52GENIChomozygous68870422
77051657670516577TC38GENICheterozygous71499050
77051667770516678CT44GENICpossibly homozygous68870428
77051675070516751CT41GENIChomozygous68870430
77051526970515270CT26GENIChomozygous70549993