chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X64341676434168AG10GENIChomozygous108437689
X64346336434634CT7GENIChomozygous108219636
X64358596435860CT7GENIChomozygous108219638
X64403996440400AG13GENIChomozygous108219642
X64406826440683AG11GENIChomozygous108219644
X64471206447121TC8GENIChomozygous108219646
X64491386449139GT13GENIChomozygous108219648
X64509576450958GA11GENIChomozygous108219651
X64511886451189AG10GENIChomozygous108219653
X64520556452056CT7GENIChomozygous108219655
X64524156452416CT4GENIChomozygous108219657
X64541066454107CT10GENIChomozygous108219659
X64557936455794AC5GENIChomozygous108219661
X64593516459352CT7GENIChomozygous108437691
X64623106462311TC7GENIChomozygous108219663
X64629316462932CA13GENIChomozygous108219665
X64658976465898AG12GENIChomozygous108219667
X64671706467171TC13GENIChomozygous108470030
X64730106473011CT8GENIChomozygous108219669
X64751196475120GT8GENIChomozygous108219672
X64757706475771GT14GENIChomozygous108219678
X64777326477733CA15GENIChomozygous108219680
X64790626479063AG12GENIChomozygous108219682
X64832716483272TG11GENIChomozygous108219684
X64837236483724GA17GENIChomozygous108219686
X64855466485547CA16GENIChomozygous108219688
X64859436485944CT8GENIChomozygous108219690
X64863176486318AC14GENIChomozygous108437693
X64881316488132GC8GENIChomozygous108219692
X64901876490188CT5GENIChomozygous108219694
X64925866492587GA9GENIChomozygous108219696
X64938896493890TC17GENIChomozygous108219698
X64982226498223GA12GENIChomozygous108219700
X64995426499543AG12GENIChomozygous108219702
X65019056501906AG14GENIChomozygous108219704
X65077386507739CG9GENIChomozygous108219709
X65107716510772AG5GENICheterozygous108219711