chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X153551526153551527CA19GENIChomozygous931019708
X153555542153555543TG15GENIChomozygous931019709
X153586538153586539TC17GENIChomozygous931019710
X153598162153598163TG12GENIChomozygous931019711
X153598807153598808GA3GENIChomozygous931019712
X153598810153598811CA3GENIChomozygous931019713
X153598870153598871CA5GENIChomozygous931019714
X153602136153602137CT11GENIChomozygous931019715
X153602157153602158CT10GENIChomozygous931019716
X153602220153602221CT7GENIChomozygous931019717
X153644951153644952TG26GENIChomozygous931019718
X153644980153644981GA19GENIChomozygous931019719
X153730942153730943TA19GENICheterozygous931019720
X153730959153730960GC18GENICheterozygous931019721
X153730961153730962AG19GENICheterozygous931019722
X153731007153731008TA14GENICpossibly homozygous931019723
X153772165153772166GT6GENIChomozygous931019724
X153814104153814105AC10GENIChomozygous931019725
X153836513153836514TG7GENIChomozygous931019726
X154010335154010336TC8GENICheterozygous931019727
X154023074154023075GT9GENIChomozygous931019728