chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4150929723150929724CCAA10GENIChomozygous58594566
4150930454150930455CT10GENIChomozygous59644694
4150930627150930628GT20GENIChomozygous59644696
4150930676150930677AT13GENIChomozygous58286320
4150931465150931466CT23GENIChomozygous56982218
4150932482150932483AC34GENIChomozygous59644698
4150932489150932490AG36GENIChomozygous56982220
4150932512150932513CT29GENIChomozygous59644700
4150932591150932592CT28GENIChomozygous59644702
4150932653150932654AT29GENIChomozygous59644704
4150932728150932729TC19GENIChomozygous59644706
4150933291150933295TGTG----6GENICheterozygous58444878
4150933293150933295TG--6GENICheterozygous58474497
4150933836150933837CT24GENIChomozygous59644708
4150934584150934585CG25GENIChomozygous59644710
4150935108150935109TC24GENIChomozygous58158267
4150935169150935170TG20GENIChomozygous59644712
4150936144150936145TC25GENIChomozygous59644714
4150936249150936250G-7GENIChomozygous59644716
4150936251150936266AGAGCAGAGCAGACA---------------7GENIChomozygous59644718
4150936341150936342CT18GENIChomozygous59644720