Please look at this NCBI page and see if this is what you are looking for.
Human Variation Sets in VCF Format
This document describes the set of files in VCF format located at ftp://ftp.ncbi.nih.gov/snp/organisms/human_9606/VCF/ . Table 1 sumarizes the files that are generated, the frequency with which they are updated, and provides an overview of the content. The names in file first column in Table 1 are linked to detailed descriptions of each file. http://www.ncbi.nlm.nih.gov/variation/docs/human_variation_vcf/
as vcf is a file format for variant calling records, it is sample specific. usually, a vcf file only contains variants sites in a genome, if you want a file contains both non-variation and variation sites of the genome, it would be very large;