chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X116768971116768972G11GENIChomozygous129782357
X116768984116768985T12GENIChomozygous129782358
X116768990116768991T14GENIChomozygous129782359
X116768994116768995AC14GENIChomozygous108313442
X116768998116768999CG14GENIChomozygous108313444
X116769021116769022T13GENIChomozygous129782360
X116769027116769028CA15GENIChomozygous108313446
X116769031116769032CA15GENIChomozygous108313448
X116769033116769034GA16GENIChomozygous108313450
X116769034116769035AG16GENIChomozygous108313452
X116777343116777344A7GENICheterozygous129782361
X116778169116778170G14GENIChomozygous129782362
X116778180116778180A13GENIChomozygous129782363
X116808178116808178A12GENIChomozygous129782364
X116784595116784595T10GENICheterozygous131970649
X116794685116794685A10GENICheterozygous131970650