chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X18754331875434CG17GENIChomozygous140602507
X18762261876227CT23GENIChomozygous147224385
X18771841877185T24GENIChomozygous147219685
X18796041879605A15GENIChomozygous140574135
X18819811881982TC4GENIChomozygous140602512
X18845351884536CT10GENIChomozygous147224386
X18848911884892TA11GENIChomozygous140602513
X18851031885104TG16GENIChomozygous140602514
X18852821885282T22GENIChomozygous140574136
X18873241887325AG8GENICheterozygous140934215
X18876341887635T11GENIChomozygous140574137
X18878941887895GA16GENIChomozygous147224387
X18881891888190CT23GENIChomozygous147224388
X18882881888289AG18GENIChomozygous140602521
X18890851889086A14GENIChomozygous140574138
X18892271889228A15GENIChomozygous140574139
X18895881889589GC17GENIChomozygous140602524
X18918431891844AG19GENICpossibly homozygous140602527
X18923031892304GA12GENIChomozygous140602528
X18923711892372A16GENIChomozygous140574140
X18938901893891AG10GENICheterozygous147765385
X18938931893894AC11GENICheterozygous147765386
X18938951893896TG10GENICheterozygous147765387
X18938981893900AG11GENICheterozygous147763976
X18939361893937TG13GENICheterozygous145974871
X18953381895339CA12GENIChomozygous147224389
X18954531895454CA15GENIChomozygous147224390
X18967431896744C9GENIChomozygous147219686
X18981441898145GA10GENIChomozygous147224391
X18987491898750TC16GENIChomozygous140602533
X19008111900811C5GENIChomozygous140574141
X19035961903597CG24GENIChomozygous147224392
X19049171904918GA21GENIChomozygous140602536
X19060991906100CA18GENIChomozygous147224393
X19062261906227CT19GENIChomozygous147224394
X18938601893861AG8GENICheterozygous403755384
X18939231893924TA13GENICheterozygous403755385
X19107331910733G25GENIChomozygous147219687
X19116861911687A25GENIChomozygous147219688