Thanks, so they were moved to archive. Actually, it will be better to use sequencing data of blood samples in vcf fomat. But when I chose "SNV" fot Data Category, it returned only "somatic mutations" files. So I thought I should use array-based genotype files!
But when I downloaded these "Annotated Somatic Mutation" files in vcf, they contain genotype column for both normal and tumor. So I guess I could use these files to get germline genotypes.
I do appreciate your answer again. It really helped!