chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71244078312440784TC24GENIChomozygous115569960
71244378212443785CCT13GENIChomozygous128435765
71244439012444391AC15GENIChomozygous115569961
71244443212444433CT20GENIChomozygous115569962
71244879512448796CA17GENIChomozygous115569963
71244889412448895GA20GENIChomozygous115569964
71244908312449084GA18GENIChomozygous115569965
71244957912449580GA12GENIChomozygous115569966
71245195612451957GA22GENIChomozygous115569967
71245200712452008GA19GENIChomozygous115569968
71245200812452009GA19GENIChomozygous115569969
71245227812452279AG14GENIChomozygous115569970
71245255412452555AG19GENIChomozygous115569971
71245412512454125A24GENIChomozygous128435766
71245421712454218CG35GENIChomozygous115569972
71245427712454278GA27GENIChomozygous115569973
71245466512454666CT35GENIChomozygous115569974
71245514412455145CT36GENIChomozygous115569975
71245515712455158GC36GENIChomozygous115569976
71245525412455255CG18GENIChomozygous115569977
71245530612455307CT19GENIChomozygous115569978
71245543612455437CG6GENIChomozygous115569979
71245552912455530CT10GENIChomozygous115569982
71245553812455539AT13GENIChomozygous115569983
71245555812455559AG14GENIChomozygous115569984
71245556912455570CT14GENIChomozygous115569985
71245565712455657T17GENICheterozygous128435767
71245581712455818CA33GENIChomozygous115569986
71245582512455826GA30GENIChomozygous115569987
71245613412456135AC32GENIChomozygous115569988
71245616812456169CT33GENIChomozygous115569989
71245736512457366TC16GENIChomozygous115569990