chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5131413965131413966GA44GENIChomozygous147544494
5131414197131414198AG44GENIChomozygous147544495
5131415136131415137TC45GENIChomozygous137622926
5131415976131415977TC53GENIChomozygous137622928
5131416339131416340TG50GENIChomozygous137622929
5131417442131417443CT49GENIChomozygous137622930
5131418041131418042GC25GENIChomozygous137622931
5131418798131418799CT29GENIChomozygous137622932
5131418808131418809AG26GENIChomozygous137622933
5131419166131419166AGC36GENIChomozygous137342143
5131415458131415458G45GENIChomozygous137342141
5131415460131415462CA45GENIChomozygous137342142
5131419299131419300GA40GENIChomozygous147544496
5131419456131419457TA40GENICpossibly homozygous137622934
5131419875131419876TA46GENIChomozygous137622935
5131420150131420151CT61GENIChomozygous147544497
5131420846131420847CT52GENIChomozygous147544498
5131420892131420893GA48GENIChomozygous147544499
5131421064131421065CT56GENIChomozygous143960629
5131421275131421276AG48GENIChomozygous147544500
5131421490131421491AT52GENIChomozygous143960630
5131422550131422551AC4GENIChomozygous143960632
5131421569131421570GA45GENIChomozygous147544501
5131421836131421837GA46GENIChomozygous147544502