chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4181434866181434867AG9GENIChomozygous112976504
4181435720181435721GA19GENIChomozygous113567361
4181435781181435782CA23GENIChomozygous113567362
4181436610181436611AG17GENIChomozygous113567363
4181436843181436844GA19GENIChomozygous112976506
4181437267181437268CT33GENIChomozygous119446561
4181437268181437269TC32GENIChomozygous119446563
4181437397181437398GA32GENIChomozygous113567364
4181441039181441040AT21GENIChomozygous113567365
4181442797181442798TC27GENIChomozygous112976527
4181443370181443371GA35GENIChomozygous113567366
4181443970181443971GT23GENIChomozygous113567367
4181445032181445033AC20GENIChomozygous112976537
4181445509181445510TG27GENIChomozygous113567368
4181446043181446044CT30GENIChomozygous113567369
4181446672181446673CT25GENIChomozygous113567370
4181448706181448707CT26GENIChomozygous113567371
4181448896181448897CT30GENIChomozygous113567372
4181452682181452683CT23GENIChomozygous113567373
4181454787181454788GA37GENICpossibly homozygous113567375
4181462026181462027CT11GENIChomozygous113567377
4181463422181463423GA32GENIChomozygous113567378
4181464930181464931TC32GENIChomozygous112976640