File 1: GWAS description, including sample size, QC, association statistic used, imputation reference panel, chip.

File 2: GWAS results. Please include information on all variants included in the association study, with the following columns:
chromosome	chromosome in hg19 coordinates 
pos	position of variant in hg19 coordinates (0-indexed)
variant	unique variant identifier (chr:pos:ref:alt)
SNP	rsID identifer
allele1	reference allele in hg19 coordinates
allele2	alternate allele in hg19 coordinates
minorallele	minor allele in cohort
maf	allele frequency of the minor allele in cohort
info	info score from imputation
beta_marginal	marginal association effect size from GWAS
se_marginal	standard error on marginal association effect size from GWAS
P	p-value from GWAS
N	sample size

File 3: Fine-mapping description, including
- Description of association analysis it is based on, as above
- Fine-mapping method used, including parameters (e.g. max #causal variants in a locus)
- How did you call loci?

File 4: Fine-mapping results. Please include information on all variants included in the fine-mapping study, with the columns described above for association, plus the following columns:
region	region of the genome fine-mapping in hg19 coordinates
pip	posterior probability of association from fine-mapping
cs_id	ID of 95% credible set (-1 indicates that variant is not in a 95% CS)
cs_pip	If the method reports a credible set-specific PIP (e.g. the alpha parameter for SuSiE) please include it. If not, omit this column.
beta_posterior	posterior expectation of true effect size
sd_posterior	posterior standard deviation of true effect size