chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5130004794130004795TC24GENIChomozygous114007514
5130004919130004920AC16GENIChomozygous114007515
5130004921130004922GC16GENIChomozygous114007516
5130007762130007763CA43GENIChomozygous114007517
5130010257130010258TC34GENIChomozygous114007518
5130010264130010265AC36GENIChomozygous114007519
5130010296130010297TC28GENIChomozygous114007520
5130011471130011472AG26GENIChomozygous114007521
5130012405130012406CT22GENIChomozygous114007522
5130013374130013375AT19GENIChomozygous114007523
5130013598130013599TC18GENIChomozygous114007524
5130013723130013724GA18GENIChomozygous114007525
5130013935130013936GC15GENIChomozygous114007526
5130015155130015156AG34GENIChomozygous114007527
5130015221130015222CT22GENICpossibly homozygous114007528
5130015316130015317CT28GENIChomozygous114007529
5130015389130015390CT19GENIChomozygous114007530
5130015890130015891TC21GENIChomozygous114007531
5130016775130016776TC21GENIChomozygous114007532
5130016937130016938CG16GENIChomozygous114007533
5130017803130017804AG28GENIChomozygous114007534
5130018846130018847TC23GENIChomozygous114007535
5130020587130020588GA28GENIChomozygous114007536
5130024037130024038TA10GENIChomozygous114007537
5130038489130038490AT31GENIChomozygous114007538
5130038521130038522AT33GENIChomozygous114007539
5130038569130038570GA24GENIChomozygous114007540
5130038794130038795AG22GENIChomozygous114007541
5130038208130038209GT21GENIChomozygous114244862
5130038836130038837CG16GENIChomozygous114007542
5130038877130038878TG14GENIChomozygous114007543
5130039454130039455AT10GENIChomozygous114007545
5130039533130039534AT5GENIChomozygous114007546
5130080575130080576TG5GENICheterozygous114007549