Additional file 1 of Ultra-low-coverage genome-wide association study—insights into gestational age using 17,844 embryo samples with preimplantation genetic testing

Additional file 1: Table S1. Genotype imputation performance at different ultra-low coverages and sample sizes. Table S2. WGA methods and sequencing platforms used in the PGT experiments. Table S3. The summary of 40 significant SNPs satisfying Bonferroni-corrected significant level of 4.526e-8. Table S4. The list of candidate SNPs. Table S5. Nonsynonymous candidate SNPs. Table S6. The reported genomic risk loci from GWAS catalog that were detected in our dataset. Table S7. A list of 166 mapped genes by positional, eQTL, and chromatin interaction mappings. Table S8. Data sources of genome-wide mRNA expression in Preterm birth, infant disease and breast cancer. Table S9. A list of the 166 mapped genes that were also identified by differentially expressed genes (DEGs) derived from analyzing the genome-wide gene expression datasets listed.