chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X116760813116760814GA18GENIChomozygous108579428
X116769027116769028CA25GENIChomozygous108313446
X116768971116768972G27GENIChomozygous129782357
X116768984116768985T23GENIChomozygous129782358
X116768990116768991T25GENIChomozygous129782359
X116769021116769022T25GENIChomozygous129782360
X116768994116768995AC25GENIChomozygous108313442
X116768998116768999CG28GENIChomozygous108313444
X116769031116769032CA27GENIChomozygous108313448
X116769033116769034GA27GENIChomozygous108313450
X116769034116769035AG27GENIChomozygous108313452
X116772755116772756GA28GENIChomozygous108579430
X116777343116777344A16GENICpossibly homozygous129782361
X116778169116778170G17GENIChomozygous129782362
X116778180116778180A20GENIChomozygous129782363
X116790369116790370AG23GENIChomozygous108579432
X116792891116792892AT23GENIChomozygous108579434
X116796843116796844GA29GENIChomozygous108579436
X116808178116808178A23GENIChomozygous129782364
X116796045116796045A29GENICpossibly homozygous131769314
X116784595116784595T24GENIChomozygous131970649
X116784765116784766G14GENIChomozygous133042517