chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69576193395761934AG14GENIChomozygous114908931
69576338195763382AT12GENIChomozygous114908932
69576391195763912AT10GENIChomozygous114908933
69576584795765848CA10GENIChomozygous114908936
69576849895768499AG24GENIChomozygous114908937
69577098595770986GA21GENIChomozygous114908940
69577402195774022AG19GENIChomozygous114908942
69577408495774085TC23GENIChomozygous115217387
69577534095775341AG15GENIChomozygous115217389
69577701595777016CT30GENIChomozygous114908945
69577794495777945AG20GENIChomozygous115217393
69577883795778838TA26GENIChomozygous115217395
69578053995780540CT30GENIChomozygous115217398
69578131795781318CA20GENIChomozygous118599383
69578352595783526CT19GENIChomozygous115217400
69578416195784162AG25GENIChomozygous114908951
69578447495784475AT15GENIChomozygous115217402
69578560095785601CT10GENIChomozygous115217404
69578811895788119AC22GENIChomozygous115217406
69578848195788482TC17GENIChomozygous115217408
69578889995788900GA17GENIChomozygous114908953
69579058395790584GA28GENIChomozygous115217409
69579413995794140GT19GENIChomozygous115217411
69579489295794893AT22GENIChomozygous115217413
69579520795795208CA22GENIChomozygous115217415
69579527395795274GA25GENIChomozygous114908957
69579588795795888AG22GENIChomozygous115217419