chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45819575658195757CT13GENIChomozygous113026037
45819586458195865GA16GENIChomozygous112660585
45819695158196952CT13GENIChomozygous112660589
45819736158197362AG8GENIChomozygous112660591
45819926158199262TC19GENIChomozygous113026038
45819945558199456TC17GENIChomozygous112660597
45820091758200918GT15GENIChomozygous113026039
45820167258201673TC25GENIChomozygous112660601
45820284058202841TG14GENIChomozygous113026040
45820326858203269TC22GENIChomozygous112660605
45820342458203425TC19GENIChomozygous112660607
45819637658196377AC19GENIChomozygous126014671
45820498158204982AG14GENIChomozygous112660611
45820502758205028TC17GENIChomozygous113026041
45820577858205779CT24GENIChomozygous113026042
45820822858208229TC16GENIChomozygous112660627
45820861658208617TC13GENIChomozygous112660629
45820878358208784CT15GENIChomozygous113026044
45820966458209665GC9GENICheterozygous113026045
45820966858209669GC9GENIChomozygous113026046
45820999858209999TA15GENIChomozygous113026047
45821002458210025GC6GENICheterozygous113026048
45821084158210842GA18GENIChomozygous113026050
45821172358211724TC6GENIChomozygous126077030
45821277758212778CT17GENIChomozygous113026051
45821430058214301TC21GENIChomozygous112660643
45821455458214555CT6GENIChomozygous113026052
45821561758215618GT18GENIChomozygous113026053
45821601858216019TC14GENIChomozygous112660647
45821606258216063CG16GENIChomozygous113026054
45821665958216660AG11GENIChomozygous113026055
45820490558204906AC4GENICheterozygous126141793