chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117048628970486289TGGT15GENIChomozygous143478841
117048629470486294T15GENICpossibly homozygous143478842
117048717570487176TG52GENIChomozygous143509691
117048758270487582A30GENIChomozygous143478843
117048784870487849CT53GENIChomozygous143509692
117048804970488050AG72GENIChomozygous143509693
117048895870488959GC32GENIChomozygous143509694
117049019370490194AG46GENIChomozygous143509695
117049020470490205CT50GENIChomozygous143509696
117049029970490300GA50GENIChomozygous143509697
117049030770490308TG50GENIChomozygous143509698
117049070270490703CT40GENIChomozygous143509701
117049040070490401GC60GENIChomozygous143509699
117049062970490630TC43GENIChomozygous143509700
117049080770490808CT53GENIChomozygous143509702
117049108970491090TC45GENIChomozygous143509703
117049119570491196TC62GENIChomozygous143509704
117049121570491216TG60GENIChomozygous143509705
117049135570491356AG51GENIChomozygous143509706
117049181770491823GTGGGG12GENIChomozygous144881162
117049198270491983AT34GENIChomozygous143509707
117049210870492109CT38GENIChomozygous143509708
117049274870492749TC43GENIChomozygous143509709
117049332370493324CA36GENIChomozygous143509710
117049360270493603CA45GENIChomozygous143509711
117049417170494172GA56GENIChomozygous143509712
117049550670495507TC55GENIChomozygous143509713
117049559570495596AG45GENIChomozygous143509714
117049567770495678GA44GENIChomozygous143509715
117049571370495720AGAGAGG45GENIChomozygous143478844
117049576270495763CT48GENIChomozygous143509716
117049591170495912AC55GENIChomozygous143509717