chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X64341676434168AG12GENIChomozygous108437689
X64346336434634CT12GENIChomozygous108219636
X64358596435860CT17GENIChomozygous108219638
X64386216438622TC8GENIChomozygous108219640
X64403996440400AG14GENIChomozygous108219642
X64406826440683AG14GENIChomozygous108219644
X64471206447121TC11GENIChomozygous108219646
X64491386449139GT13GENIChomozygous108219648
X64509576450958GA12GENIChomozygous108219651
X64511886451189AG8GENIChomozygous108219653
X64520556452056CT10GENICpossibly homozygous108219655
X64524156452416CT9GENIChomozygous108219657
X64541066454107CT18GENIChomozygous108219659
X64557936455794AC11GENIChomozygous108219661
X64593516459352CT13GENIChomozygous108437691
X64623106462311TC15GENIChomozygous108219663
X64629316462932CA10GENIChomozygous108219665
X64658976465898AG12GENIChomozygous108219667
X64730106473011CT15GENIChomozygous108219669
X64751196475120GT18GENIChomozygous108219672
X64757706475771GT17GENIChomozygous108219678
X64777326477733CA13GENIChomozygous108219680
X64790626479063AG9GENIChomozygous108219682
X64832716483272TG10GENIChomozygous108219684
X64837236483724GA12GENIChomozygous108219686
X64855466485547CA19GENIChomozygous108219688
X64859436485944CT20GENIChomozygous108219690
X64863176486318AC12GENIChomozygous108437693
X64881316488132GC11GENIChomozygous108219692
X64901876490188CT6GENIChomozygous108219694
X64925866492587GA12GENIChomozygous108219696
X64938896493890TC19GENIChomozygous108219698
X64982226498223GA19GENICpossibly homozygous108219700
X64995426499543AG20GENIChomozygous108219702
X65019056501906AG20GENIChomozygous108219704
X65050076505008CA10GENIChomozygous108219706
X65077386507739CG7GENIChomozygous108219709
X65107716510772AG16GENIChomozygous108219711
X65272496527250AT12GENIChomozygous108219716