chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172605623172605624TG6GENIChomozygous114092829
5172605712172605715TGT10GENIChomozygous128276580
5172605821172605821A7GENIChomozygous128276581
5172605822172605823GA7GENIChomozygous119023072
5172605843172605844GA8GENIChomozygous114092831
5172605863172605864G9GENIChomozygous128276582
5172605870172605871A9GENIChomozygous128276583
5172605872172605873G9GENIChomozygous128276584
5172605892172605893G10GENIChomozygous128276585
5172605904172605905TG9GENIChomozygous114092833
5172605932172605932T8GENIChomozygous128276586
5172605943172605943A7GENIChomozygous128276587
5172605976172605977G1GENIChomozygous128276588
5172606090172606090C6GENIChomozygous128276592
5172606111172606112T8GENIChomozygous128276593
5172606117172606118G8GENIChomozygous128276594
5172606139172606140TG10GENIChomozygous114092837
5172606141172606142G10GENIChomozygous128276595
5172606149172606150G10GENIChomozygous128276596
5172606215172606216GT13GENIChomozygous118848114
5172606216172606217TA12GENIChomozygous114092839
5172606453172606454C10GENIChomozygous128276597
5172610849172610850C5GENIChomozygous128276601
5172622875172622876T7GENIChomozygous128276605
5172622876172622877GA7GENIChomozygous118938120
5172622878172622879TC7GENIChomozygous118938122
5172622879172622880TC7GENIChomozygous118938124