VCFs: See 1000 Genomes on GRCh38 for vcf data. Files are expected to be divided by sample rather than by chromosome. Do this yourself, or run this otherwise deprecated script to produce 1000 genomes vcf files divided by sample, but covering chromosome 22 only (in GRCh37).
Bigwigs: Bigwig files referred to in the dataset are downloable from IHEC here: (1 2 3)