chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87922913979229140AG21GENIChomozygous117145560
87923018779230188TC31GENIChomozygous117948305
87923028079230281TC33GENICpossibly homozygous117948306
87923182679231827AT23GENIChomozygous117948307
87923200379232004CG27GENIChomozygous117948308
87923374879233749AG13GENIChomozygous117948309
87923521079235211CT19GENIChomozygous117948310
87923693379236934AG8GENIChomozygous117145561
87924146579241466AT11GENICpossibly homozygous118104403
87924263979242640AG29GENIChomozygous117948311
87924374379243744CT21GENIChomozygous117948312
87924550079245501CT14GENIChomozygous117145562
87924563179245632GA20GENIChomozygous117948314
87924642079246421GA23GENIChomozygous117948315
87924739679247397AT34GENIChomozygous117948316
87924966379249664TC14GENIChomozygous117948318
87925110679251107GA31GENIChomozygous117145564
87925374379253744AC18GENIChomozygous117145567
87925537479255375TA30GENIChomozygous118104405
87925540279255403AT29GENIChomozygous118104407
87925609779256098CT18GENIChomozygous117948319
87925633279256333CA17GENIChomozygous118104409
87925729479257295TC22GENIChomozygous117948320
87926092979260930GT39GENIChomozygous117948322
87926098179260982GA35GENIChomozygous117948323
87926478879264789AG32GENIChomozygous117948324
87927077779270778AC15GENIChomozygous117145573
87927113979271140GA25GENIChomozygous117948325
87927172779271728TC20GENIChomozygous117145575
87927288079272881AG24GENIChomozygous117948327
87927370179273702TC15GENIChomozygous116971455
87927435079274351GA34GENIChomozygous117046857
87927714579277146TG31GENIChomozygous117948328
87927859279278593AT24GENIChomozygous117948329