chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4158110101158110102CT50GENIChomozygous137249414
4158110674158110674GTGTGTGT60GENIChomozygous136925444
4158110676158110676GTGTGT61GENIChomozygous136925445
4158110718158110719CT60GENICpossibly homozygous137249415
4158111131158111132GA41GENIChomozygous137249416
4158111297158111298GA62GENIChomozygous137249417
4158111866158111867CT57GENIChomozygous137249418
4158111878158111879CT57GENIChomozygous137249419
4158112592158112593TC49GENIChomozygous137249420
4158113686158113687AG78GENIChomozygous137249421
4158115264158115265TC56GENIChomozygous137249422
4158110981158110982C45GENIChomozygous403125319
4158110981158110982CT45GENICheterozygous403125320