Below is a description of the variant data analyzed in Szpiech et al. (2013). Genomic coordinates are given with respect to human reference assembly hg18.

Citations:
(1) ZA Szpiech, J Xu, TJ Pemberton, W Peng, S Zöllner, NA Rosenberg, JZ Li (2013) Long runs of homozygosity are enriched for deleterious variation. American Journal of Human Genetics 93: 90-102.


FILE: coding_variants_hgdp27.vcf
      This file contains genotype information for all synonymous and missense variants in the following format:

      <Header>
      <chr>   <pos>	<reference allele>	<alternate allele>	<functional classification>	<genotype0>	... <genotype26>
      ...

FILE: coding_variants_nonsense_hgdp27.vcf
      This file contains genotype information for all nonsense variants in the following format:

      <Header>
      <chr>   <pos>	<reference allele>	<alternate allele>	<functional classification>	<genotype0>	... <genotype26>
      ...

