chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7576286975762870GGA34GENIChomozygous45151436
X7577446475774466CT--11GENICpossibly homozygous45151437
X7578446575784468AAT---33GENICpossibly homozygous45151438
X7578977675789777T-14GENICheterozygous45260830
X7579403375794034AG11GENICheterozygous45260831
X7579779475797796AC--40GENICheterozygous45151440
X7580407175804073AC--24GENICheterozygous45151441
X7580407475804075CG36GENICpossibly homozygous45151442
X7580868975808692CCC---7GENICheterozygous45260832
X7580869175808692C-7GENICheterozygous45260833
X7581665475816655G-40GENIChomozygous45151444
X7582907175829072A-16GENIChomozygous45151446
X7582908775829088A-14GENIChomozygous45151447
X7582910275829103G-10GENIChomozygous45151448
X7582911975829120GT16GENIChomozygous45151449
X7582912775829128T-17GENIChomozygous45151450
X7582913875829139AC18GENIChomozygous45151451
X7582915375829154CT22GENIChomozygous45151452
X7582916075829161C-21GENIChomozygous45151453
X7582916575829166GC21GENIChomozygous45151454
X7582917075829171AAC20GENIChomozygous45151456
X7582917375829174CT21GENIChomozygous45260834
X7582917675829177AC23GENIChomozygous45151457
X7582918175829182A-22GENIChomozygous45151458
X7582918575829186AT23GENIChomozygous45151459
X7582918875829189GC23GENIChomozygous45151460
X7583065075830651TC23GENICheterozygous45260835
X7583124375831244AC154GENICheterozygous45151462
X7584073275840734AC--10GENIChomozygous45151463