chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104926187449261875TC34GENIChomozygous116931973
104926203849262039AG19GENIChomozygous116882244
104926215549262156AG17GENIChomozygous116882246
104926310349263104CT22GENIChomozygous116931975
104926407949264080AG19GENIChomozygous116931977
104926430249264303TC25GENIChomozygous116882248
104926477449264775AC13GENIChomozygous116588718
104926483049264831TG24GENIChomozygous116588720
104926878249268783TA25GENIChomozygous117059183
104926878349268784CT25GENIChomozygous116882250
104926894849268949TG25GENIChomozygous117009401
104926897149268972GC27GENIChomozygous116588726
104927173949271740GA21GENIChomozygous116931979
104927336649273367AG18GENIChomozygous116882258
104927398449273985TC24GENIChomozygous116882264
104927486949274870CT28GENIChomozygous116931981
104927507049275071CT23GENIChomozygous116882266
104927528749275288CT22GENIChomozygous116931983
104927533649275337AG19GENIChomozygous116882268
104927539049275391GA19GENIChomozygous116931985
104927555049275551AG24GENIChomozygous116882270
104927569149275692GA19GENIChomozygous116931987
104927690749276908AG34GENIChomozygous116931989
104927853349278534CT21GENIChomozygous116931991
104928146949281470GA26GENIChomozygous116882306
104928309149283092GT27GENIChomozygous116931993
104928405049284051AG22GENIChomozygous116931995
104928783649287837CT27GENIChomozygous116931997
104928846649288467GA26GENIChomozygous116931999
104928877849288779GA39GENIChomozygous116932001
104929196049291961CA27GENIChomozygous116588736
104929200649292007AT24GENIChomozygous116588738
104929200749292008TA24GENIChomozygous116588740
104929207349292074AT25GENIChomozygous116932003
104929333049293331CT21GENIChomozygous116932005
104929546449295465CT28GENIChomozygous116932007
104929563349295634AG38GENIChomozygous116882336
104928511049285111TA21GENIChomozygous116977680