chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5130003755130003756GT20GENIChomozygous118845495
5130003756130003757TG20GENIChomozygous118845496
5130004794130004795TC33GENICpossibly homozygous114007514
5130004921130004922GC30GENIChomozygous114007516
5130007762130007763CA22GENIChomozygous114007517
5130010257130010258TC38GENIChomozygous114007518
5130010264130010265AC43GENIChomozygous114007519
5130010296130010297TC41GENIChomozygous114007520
5130011471130011472AG25GENIChomozygous114007521
5130012405130012406CT27GENIChomozygous114007522
5130013374130013375AT43GENIChomozygous114007523
5130013598130013599TC31GENIChomozygous114007524
5130013723130013724GA24GENIChomozygous114007525
5130013935130013936GC23GENIChomozygous114007526
5130015155130015156AG22GENIChomozygous114007527
5130015221130015222CT25GENICpossibly homozygous114007528
5130015316130015317CT25GENIChomozygous114007529
5130015389130015390CT17GENIChomozygous114007530
5130015890130015891TC33GENIChomozygous114007531
5130016775130016776TC35GENIChomozygous114007532
5130016937130016938CG21GENIChomozygous114007533
5130017803130017804AG26GENIChomozygous114007534
5130018846130018847TC14GENIChomozygous114007535
5130020587130020588GA37GENIChomozygous114007536
5130079979130079980GA22GENIChomozygous118845500