chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103636217436362175TC28GENIChomozygous116759049
103636313336363134AG14GENIChomozygous116560613
103636323936363240TC13GENIChomozygous116560617
103636392236363923TC20GENIChomozygous116759051
103636478936364790AG24GENIChomozygous116560619
103636554536365546CT24GENIChomozygous116759053
103636593836365939AG21GENIChomozygous116560627
103636656536366566AG6GENIChomozygous116759057
103636726236367263AG26GENIChomozygous116759059
103636787236367873TC25GENIChomozygous116560629
103636797436367975CT32GENIChomozygous116759061
103636832436368325AG22GENIChomozygous116759063
103636841336368414TA30GENIChomozygous116560631
103636878736368788AG19GENIChomozygous116560635
103637050536370506TA30GENIChomozygous116759067
103637073236370733CG27GENIChomozygous116759069
103637077236370773AG27GENIChomozygous116759071
103637222836372229CG17GENIChomozygous116759073
103637231836372319TC23GENIChomozygous116560639
103637240536372406GA21GENIChomozygous116759075
103637243836372439TC20GENIChomozygous116560641
103637247136372472TC21GENIChomozygous116560643
103637326836373269GA21GENIChomozygous116759077
103637329936373300AC19GENIChomozygous116759079
103637346636373467TC2GENIChomozygous117390959
103637347436373475CT2GENIChomozygous117390961
103637390136373902CT25GENIChomozygous116759081
103637397836373979TC23GENIChomozygous116759083
103637417936374180AG21GENIChomozygous116759085
103637429736374298GC17GENIChomozygous116759087
103637485636374857GA9GENIChomozygous117124407
103637489936374900GA11GENIChomozygous117124409
103637529936375300TA17GENIChomozygous116759089
103637541836375419GA12GENIChomozygous116759091
103637553536375536CG14GENIChomozygous116759093
103637609936376100GA21GENIChomozygous116759095
103637714436377145AG44GENIChomozygous116759097