chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X64358596435860CT15GENIChomozygous108219638
X64386216438622TC12GENIChomozygous108219640
X64406826440683AG13GENIChomozygous108219644
X64471206447121TC17GENIChomozygous108219646
X64491386449139GT14GENIChomozygous108219648
X64509576450958GA17GENIChomozygous108219651
X64511886451189AG7GENIChomozygous108219653
X64520556452056CT19GENIChomozygous108219655
X64557936455794AC16GENIChomozygous108219661
X64623106462311TC18GENIChomozygous108219663
X64629316462932CA17GENIChomozygous108219665
X64658976465898AG22GENIChomozygous108219667
X64730106473011CT18GENIChomozygous108219669
X64751196475120GT20GENIChomozygous108219672
X64757706475771GT24GENIChomozygous108219678
X64777326477733CA13GENIChomozygous108219680
X64790626479063AG20GENIChomozygous108219682
X64832716483272TG13GENIChomozygous108219684
X64837236483724GA20GENIChomozygous108219686
X64855466485547CA20GENIChomozygous108219688
X64859436485944CT16GENIChomozygous108219690
X64863176486318AC15GENIChomozygous108437693
X64881316488132GC8GENIChomozygous108219692
X64901876490188CT22GENIChomozygous108219694
X64925866492587GA14GENIChomozygous108219696
X64938896493890TC21GENIChomozygous108219698
X64982226498223GA22GENIChomozygous108219700
X65019056501906AG17GENIChomozygous108219704
X64929256492926TC18GENIChomozygous108539133