chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117048628970486289TGGT22GENIChomozygous143478841
117048629470486294T15GENIChomozygous143478842
117048717570487176TG40GENIChomozygous143509691
117048758270487582A23GENIChomozygous143478843
117048784870487849CT40GENIChomozygous143509692
117048804970488050AG56GENIChomozygous143509693
117048895870488959GC34GENIChomozygous143509694
117049019370490194AG48GENIChomozygous143509695
117049020470490205CT44GENIChomozygous143509696
117049029970490300GA45GENIChomozygous143509697
117049030770490308TG45GENIChomozygous143509698
117049040070490401GC45GENIChomozygous143509699
117049062970490630TC39GENIChomozygous143509700
117049070270490703CT44GENIChomozygous143509701
117049080770490808CT52GENIChomozygous143509702
117049108970491090TC62GENIChomozygous143509703
117049119570491196TC71GENIChomozygous143509704
117049121570491216TG68GENIChomozygous143509705
117049135570491356AG30GENIChomozygous143509706
117049181770491823GTGGGG5GENIChomozygous144881162
117049198270491983AT34GENIChomozygous143509707
117049210870492109CT27GENIChomozygous143509708
117049274870492749TC27GENIChomozygous143509709
117049332370493324CA48GENIChomozygous143509710
117049360270493603CA43GENIChomozygous143509711
117049417170494172GA52GENIChomozygous143509712
117049550670495507TC46GENIChomozygous143509713
117049559570495596AG36GENIChomozygous143509714
117049567770495678GA30GENIChomozygous143509715
117049571370495720AGAGAGG28GENIChomozygous143478844
117049576270495763CT39GENIChomozygous143509716
117049591170495912AC43GENIChomozygous143509717