chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141125670311256704CG36GENIChomozygous813654963
141125708911257090CT25GENICpossibly homozygous813654964
141125980911259810AG19GENIChomozygous813654965
141126066411260665AT17GENIChomozygous813654966
141126069711260698CT13GENIChomozygous813654967
141126187911261880AG35GENIChomozygous813654968
141126237211262373TC17GENIChomozygous813654969
141126243111262432GA26GENIChomozygous813654970
141126243311262434CT26GENIChomozygous813654971
141126350911263510AT12GENIChomozygous813654972
141126364911263650CT13GENIChomozygous813654973
141126387311263874CT19GENICheterozygous813654974
141126416011264161TC30GENIChomozygous813654975
141126456711264568TC26GENIChomozygous813654976
141126462111264622GA18GENIChomozygous813654977
141126503211265033TA35GENIChomozygous813654978
141126524911265250CG34GENIChomozygous813654979
141126540111265402GA16GENIChomozygous813654980
141126608411266085CT22GENIChomozygous813654981
141126679111266792TC16GENIChomozygous813654982
141126769511267696CT17GENIChomozygous813654983
141126771711267718CA14GENICheterozygous813654984
141126771911267720CA11GENICpossibly homozygous813654985
141126897811268979AG31GENIChomozygous813654986
141126934911269350GC15GENIChomozygous813654987
141126936611269367GA20GENIChomozygous813654988
141126937911269380CT19GENIChomozygous813654989
141126939511269396GA20GENIChomozygous813654990
141126944411269445CT21GENIChomozygous813654991
141126945511269456GA18GENIChomozygous813654992
141126998411269985TC22GENIChomozygous813654993
141127047311270474GA17GENIChomozygous813654994
141127080111270802AG21GENIChomozygous813654995
141127133911271340TC13GENIChomozygous813654996
141127277511272776GA17GENIChomozygous813654997
141127279011272791CT16GENIChomozygous813654998
141127358511273586TC17GENIChomozygous813654999