Easily sort long list of genomic coordinates into coding/noncoding

Hi All,

I have downloaded all possible indels/snv files from CADD and I wanted to know if there is an easy way to use a VCF file as an input and will get where the variant is on the genome (ie in a coding region/noncoding).

cadd genomic coordinates

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written 6.0 years ago by skk478 •

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