Candidate SNPs confirmed through Sanger sequencing.

SNPs are labeled with the appropriate IUB ambiguity code. The SNPs that were confirmed in individual samples as well as the pooled sample are in bold. The major and minor allele frequencies are given.

Figshare2015-12-02 更新10

Candidate risk variants identified in GWAS confirmed by Sanger sequencing.

Figshare2018-03-17 更新00

SNP validation with Sanger sequencing.

“False” – number of false positives, “% False” – percentage of false positives. “15–40 fold” and “>40 fold” - indicate the groups of SNPs with different sequence coverage. “35–50% het”, “35–50% het” a

NIAID Data Ecosystem20