chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71244078312440784TC78GENIChomozygous115569960
71244439012444391AC77GENIChomozygous115569961
71244443212444433CT78GENIChomozygous115569962
71244879512448796CA86GENIChomozygous115569963
71244889412448895GA83GENIChomozygous115569964
71244908312449084GA74GENIChomozygous115569965
71244957912449580GA60GENIChomozygous115569966
71245195612451957GA62GENIChomozygous115569967
71245200712452008GA48GENIChomozygous115569968
71245200812452009GA47GENIChomozygous115569969
71244378212443785CCT68GENIChomozygous128435765
71245227812452279AG86GENIChomozygous115569970
71245255412452555AG69GENIChomozygous115569971
71245412512454125A64GENICpossibly homozygous128435766
71245421712454218CG84GENIChomozygous115569972
71245427712454278GA67GENIChomozygous115569973
71245466512454666CT84GENIChomozygous115569974
71245514412455145CT74GENIChomozygous115569975
71245515712455158GC69GENIChomozygous115569976
71245525412455255CG71GENIChomozygous115569977
71245530612455307CT78GENIChomozygous115569978
71245543612455437CG33GENIChomozygous115569979
71245547912455480TC34GENIChomozygous115569981
71245552912455530CT58GENIChomozygous115569982
71245553812455539AT59GENIChomozygous115569983
71245555812455559AG60GENIChomozygous115569984
71245556912455570CT63GENIChomozygous115569985
71245565712455657T36GENICheterozygous128435767
71245581712455818CA99GENIChomozygous115569986
71245582512455826GA97GENIChomozygous115569987
71245613412456135AC92GENIChomozygous115569988
71245616812456169CT100GENIChomozygous115569989
71245736512457366TC33GENIChomozygous115569990