chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113171991631719917CT33GENIChomozygous964763651
113172086931720870AG31GENIChomozygous964763652
113172127731721278GA17GENIChomozygous964763653
113172270531722706TA18GENIChomozygous964763654
113172385431723855GA29GENIChomozygous964763655
113172416031724161CG32GENIChomozygous964763656
113172470331724704AC31GENIChomozygous964763657
113172824931728250CA12GENIChomozygous964763658
113173103631731037CT18GENIChomozygous964763659
113173257431732575CT40GENIChomozygous964763660
113173276931732770TC38GENIChomozygous964763661
113173279931732800AG40GENIChomozygous964763662
113173446031734461AG27GENIChomozygous964763663
113173630931736310GA30GENIChomozygous964763664
113173680031736801TC31GENIChomozygous964763665
113173794831737949AG25GENIChomozygous964763666
113173857731738578CT31GENIChomozygous964763667
113174057731740578GA38GENIChomozygous964763668
113174185231741853GA32GENIChomozygous964763669
113174362231743623AT35GENIChomozygous964763670
113174391731743918GA20GENIChomozygous964763671
113174552431745525CT14GENIChomozygous964763672
113174664231746643CG19GENIChomozygous964763673
113174740931747410AT16GENIChomozygous964763674
113174928231749283AT27GENIChomozygous964763675
113174963131749632GA24GENIChomozygous964763676
113174984131749842TC33GENIChomozygous964763677
113175017931750180GA24GENIChomozygous964763678