chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X153551526153551527CA19GENIChomozygous108353735
X153555542153555543TG15GENIChomozygous108353737
X153586538153586539TC17GENIChomozygous108353739
X153598162153598163TG12GENIChomozygous108353741
X153598807153598808GA3GENIChomozygous108353743
X153598810153598811CA3GENIChomozygous108353745
X153598870153598871CA5GENIChomozygous108353747
X153602136153602137CT11GENIChomozygous108353749
X153602157153602158CT10GENIChomozygous108353751
X153602220153602221CT7GENIChomozygous108353753
X153644951153644952TG26GENIChomozygous108353755
X153644980153644981GA19GENIChomozygous108353757
X153730942153730943TA19GENICheterozygous108353759
X153730959153730960GC18GENICheterozygous108353761
X153730961153730962AG19GENICheterozygous108353763
X153731007153731008TA14GENICpossibly homozygous108353765
X153772165153772166GT6GENIChomozygous108353767
X153814104153814105AC10GENIChomozygous108353770
X153836513153836514TG7GENIChomozygous108353772
X154010335154010336TC8GENICheterozygous108353774
X154023074154023075GT9GENIChomozygous108353776