chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X64341676434168AG30GENIChomozygous108437689
X64346336434634CT17GENIChomozygous108219636
X64358596435860CT18GENIChomozygous108219638
X64386216438622TC22GENIChomozygous108219640
X64403996440400AG26GENIChomozygous108219642
X64406826440683AG34GENIChomozygous108219644
X64471206447121TC31GENIChomozygous108219646
X64491386449139GT24GENIChomozygous108219648
X64509576450958GA26GENIChomozygous108219651
X64511886451189AG20GENIChomozygous108219653
X64520556452056CT14GENIChomozygous108219655
X64541066454107CT17GENIChomozygous108219659
X64557936455794AC16GENIChomozygous108219661
X64593516459352CT11GENIChomozygous108437691
X64623106462311TC26GENIChomozygous108219663
X64629316462932CA29GENIChomozygous108219665
X64658976465898AG20GENIChomozygous108219667
X64671706467171TC24GENIChomozygous108470030
X64730106473011CT23GENIChomozygous108219669
X64751196475120GT23GENIChomozygous108219672
X64757706475771GT25GENIChomozygous108219678
X64777326477733CA39GENIChomozygous108219680
X64790626479063AG39GENIChomozygous108219682
X64832716483272TG22GENIChomozygous108219684
X64837236483724GA25GENIChomozygous108219686
X64855466485547CA26GENIChomozygous108219688
X64859436485944CT19GENIChomozygous108219690
X64863176486318AC28GENIChomozygous108437693
X64881316488132GC24GENIChomozygous108219692
X64901876490188CT6GENIChomozygous108219694
X64925866492587GA36GENIChomozygous108219696
X64938896493890TC29GENIChomozygous108219698
X64982226498223GA30GENIChomozygous108219700
X64995426499543AG28GENIChomozygous108219702
X65019056501906AG23GENIChomozygous108219704
X65050076505008CA5GENIChomozygous108219706
X65077386507739CG24GENIChomozygous108219709
X65107716510772AG21GENIChomozygous108219711
X65272496527250AT17GENIChomozygous108219716