chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3100513165100513166TC59GENIChomozygous141519400
3100513289100513290CT69GENIChomozygous141519401
3100513333100513334GA76GENIChomozygous141519402
3100513474100513475GA57GENIChomozygous141519403
3100514096100514097GA59GENIChomozygous141519404
3100514277100514278CG55GENIChomozygous141519405
3100514385100514386AG42GENIChomozygous141519406
3100514490100514491TA55GENIChomozygous141519407
3100514849100514850AG61GENIChomozygous141519408
3100515146100515147AT58GENIChomozygous141519409
3100518857100518858GA46GENICpossibly homozygous154127425
3100519976100519977CT50GENIChomozygous141519410
3100522048100522049CG22GENIChomozygous141519413
3100523618100523619TA62GENIChomozygous141519414
3100518857100518858G46GENICheterozygous145395305
3100520852100520853C30GENIChomozygous403071710
3100520852100520853CT30GENICheterozygous403071711
3100522056100522057C19GENICheterozygous403071713
3100522056100522057CG19GENIChomozygous403071714
3100520833100520865TTATTTATTTATTTATTTACTTACTTACTTAC30GENIChomozygous141477379