chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86337001863370019T-44GENIChomozygous737705226
86337339863373399CT30GENIChomozygous614508642
86337560863375609TC55GENIChomozygous614508643
86337966563379666CA25GENIChomozygous614508644
86337999863379999GGGTGTGT2GENIChomozygous737705229
86338127063381271GA27GENIChomozygous614508645
86338200663382007GA20GENIChomozygous614508646
86338517163385172GGCACACA12GENIChomozygous737705233
86338626763386268TC27GENIChomozygous614508647
86338676663386767TC35GENIChomozygous614508648
86339087763390878TC35GENIChomozygous614508649
86339242763392428AG15GENIChomozygous614508650
86339330663393307CT30GENIChomozygous614508651
86339420063394201AG23GENIChomozygous614508652
86339494763394948TG16GENIChomozygous614508653
86339496363394966TTT---11GENICheterozygous737705234
86339496463394966TT--11GENICheterozygous737705235
86339503463395035C-19GENIChomozygous737705238
86339510263395103GGA15GENICpossibly homozygous737705239
86339510263395103GGAA15GENICheterozygous737705240
86339628063396281TC35GENIChomozygous614508654
86339827963398280GA19GENIChomozygous614508655
86340095563400956TC18GENIChomozygous614508656
86340189063401891TC24GENIChomozygous614508657
86340203963402040GA26GENIChomozygous614508658
86340215863402159TC21GENIChomozygous614508659
86340238263402383CCT13GENIChomozygous737705241
86340305863403059TA39GENIChomozygous614508660