chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104779636147796362CT21GENIChomozygous116587881
104779715947797160GC18GENIChomozygous116587885
104779752647797527TA29GENIChomozygous116878935
104779789247797893AG14GENIChomozygous116587887
104779984947799850TG10GENIChomozygous116587889
104779985047799851TC11GENIChomozygous116587891
104780145847801459TC34GENIChomozygous116587893
104780395947803960AG26GENIChomozygous116587895
104780677547806776AG12GENIChomozygous117410527
104780807547808076TG20GENIChomozygous116587897
104780859947808600CA16GENIChomozygous116587901
104780881047808811CG12GENIChomozygous116878937
104780889847808899TG20GENIChomozygous116587903
104781330447813305GA12GENIChomozygous116587905
104781331847813319GC8GENIChomozygous116878939
104781332947813330CG16GENIChomozygous116587907
104781384347813844AG16GENIChomozygous116878941
104781873247818733GT15GENIChomozygous116878943
104782565547825656AC21GENIChomozygous116587913
104782730647827307GA17GENIChomozygous116587917
104782956747829568CT25GENIChomozygous116587921
104783260147832602TA19GENIChomozygous116587923
104783261947832620CT21GENIChomozygous116587925
104783420547834206CT22GENIChomozygous116878945
104784157847841579CT21GENIChomozygous116878947
104784345847843459TG3GENICheterozygous126430891
104784377247843773CT22GENIChomozygous116878949
104784723747847238CA34GENIChomozygous116587937
104784887147848872GA10GENIChomozygous116878951
104784946747849468AG11GENIChomozygous116587941
104784968347849684TC32GENIChomozygous116587943
104785243547852436AC15GENIChomozygous116587947
104785294947852950CT9GENIChomozygous117008959
104785315247853153CA16GENIChomozygous116587949
104785464147854642GA17GENIChomozygous116878953
104785577947855780TC10GENIChomozygous116587953
104785578647855787TC14GENIChomozygous116587955