chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X18754331875434CG13GENIChomozygous140602507
X18762261876227CT16GENIChomozygous147224385
X18771841877185T17GENIChomozygous147219685
X18796041879605A5GENIChomozygous140574135
X18819811881982TC6GENIChomozygous140602512
X18845351884536CT11GENIChomozygous147224386
X18848911884892TA18GENIChomozygous140602513
X18851031885104TG15GENIChomozygous140602514
X18852821885282T13GENIChomozygous140574136
X18876341887635T10GENIChomozygous140574137
X18878941887895GA9GENIChomozygous147224387
X18881891888190CT11GENIChomozygous147224388
X18882881888289AG14GENIChomozygous140602521
X18890851889086A9GENIChomozygous140574138
X18892271889228A15GENIChomozygous140574139
X18895881889589GC15GENIChomozygous140602524
X18918431891844AG19GENIChomozygous140602527
X18923031892304GA6GENIChomozygous140602528
X18923711892372A4GENIChomozygous140574140
X18953381895339CA7GENIChomozygous147224389
X18954531895454CA15GENICpossibly homozygous147224390
X18967431896744C5GENIChomozygous147219686
X18981441898145GA12GENIChomozygous147224391
X18987491898750TC11GENIChomozygous140602533
X19008111900811C2GENIChomozygous140574141
X19035961903597CG20GENIChomozygous147224392
X19049171904918GA16GENIChomozygous140602536
X19060991906100CA17GENIChomozygous147224393
X19062261906227CT19GENIChomozygous147224394
X19107331910733G16GENIChomozygous147219687
X19116861911687A32GENIChomozygous147219688
X18819811881982T6GENICheterozygous403473606