chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151112973151112974A-12GENICheterozygous55924204
5151116881151116882TG50GENICheterozygous55795488
5151116905151116906TC52GENICheterozygous55795489
5151116918151116919CG43GENICheterozygous55795492
5151116931151116932CT46GENICheterozygous55795493
5151117470151117471TC32GENICpossibly homozygous55795495
5151118203151118204A-55GENIChomozygous55795497
5151122249151122253CTTC----19GENIChomozygous55795507
5151128281151128282TG41GENIChomozygous55924206
5151129721151129722TTACAC9GENICheterozygous55795518
5151129721151129722TTAC9GENICheterozygous55924208
5151132099151132103TATG----12GENICheterozygous55795522
5151133191151133192AG77GENIChomozygous55924210