chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138380757083807571CT43GENIChomozygous782026329
138381126883811269TC56GENIChomozygous782026330
138381272483812725GA21GENICpossibly homozygous782026331
138381327283813273GA56GENIChomozygous782026332
138381452283814523CT58GENIChomozygous782026333
138381557483815575CA62GENIChomozygous782026334
138381692183816922TC63GENIChomozygous782026335
138381912283819123AT81GENIChomozygous782026336
138382161383821614GT57GENIChomozygous782026337
138382177683821777GC48GENIChomozygous782026338
138382471483824715GA58GENICpossibly homozygous782026339
138382518483825185CT64GENIChomozygous782026340
138382678083826781GA62GENIChomozygous782026341
138382777383827774GA51GENIChomozygous782026342
138382781583827816CT55GENIChomozygous782026343
138382841683828417TG40GENIChomozygous782026344
138382857883828579TG53GENIChomozygous782026345
138383067483830675GA83GENICheterozygous782026346
138383126983831270AG40GENIChomozygous782026347
138383127583831276AG42GENIChomozygous782026348
138383128183831282AG44GENIChomozygous782026349
138383129383831294AG49GENIChomozygous782026350
138383129983831300AG50GENIChomozygous782026351
138383130583831306AG50GENIChomozygous782026352
138383136683831367TC59GENICpossibly homozygous782026353
138383420883834209GA57GENIChomozygous782026354
138383433183834332AG48GENIChomozygous782026355
138383514083835141AG44GENIChomozygous782026356
138383615483836155AG66GENIChomozygous782026357
138383686283836863TA75GENIChomozygous782026358
138383779883837799CG58GENIChomozygous782026359
138383878383838784TC49GENIChomozygous782026360
138383971383839714GA70GENIChomozygous782026361
138384199383841994CG41GENIChomozygous782026362
138384201083842011CA42GENIChomozygous782026363