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Find SNPs which disrupt CpG sites

Hi, I have a vcf file and I want to find which variants disrupt a CpG site (given by a matching fasta file). I'm sure there is an easy way to do this, but does anyone have any suggestions?

I'd settle for a way to annotate the location of each CpG site from the fasta file, which I could then intersect with the vcf file.

Thanks!

vcf genome variants

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