chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7576086275760863GGT5GENICheterozygous45325198
X7578446575784471AATAAT------1GENIChomozygous45588459
X7579955075799551T-6GENICheterozygous45569996
X7576286975762870GGA11GENIChomozygous45151436
X7577447275774476CTCT----1GENIChomozygous45548062
X7576900575769007GT--5GENICheterozygous45512940
X7577175775771759AC--8GENICheterozygous45512942
X7579695275796953GGAC1GENIChomozygous45649832
X7580407375804075AC--3GENICheterozygous45512946
X7580869175808692C-7GENICheterozygous45260833
X7581665475816655G-18GENIChomozygous45151444
X7582907175829072A-11GENIChomozygous45151446
X7582908775829088A-14GENIChomozygous45151447
X7582910275829103G-12GENIChomozygous45151448
X7582911975829120GT16GENIChomozygous45151449
X7582912775829128T-16GENIChomozygous45151450
X7582913875829139AC12GENIChomozygous45151451
X7582915375829154CT10GENIChomozygous45151452
X7582916075829161C-8GENIChomozygous45151453
X7582916575829166GC7GENIChomozygous45151454
X7582916875829169AC7GENIChomozygous45151455
X7582917075829171AAC7GENIChomozygous45151456
X7582917375829174CT7GENIChomozygous45260834
X7582917675829177AC7GENIChomozygous45151457
X7582918175829182A-7GENIChomozygous45151458
X7582918575829186AT7GENIChomozygous45151459
X7582918875829189GC6GENIChomozygous45151460
X7583644275836443A-11GENICheterozygous45548066
X7584073275840734AC--3GENICheterozygous45151463