ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR424/005/SRR4240525/SRR4240525.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR424/007/SRR4240527/SRR4240527.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR424/006/SRR4240526/SRR4240526.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR424/008/SRR4240528/SRR4240528.fastq.gzprimaryOK200GenomicsDepartment of Pediatrics, University of Chicagohttps://www.ebi.ac.uk/ena/browser/view/PRJNA342773Mus musculusxref:PubMed:28240319ChIP-seq targeting H3K9ac and H3K27me3 histone modifications was carried out on macrophages isolated from aortas of mice exposed to intermittent hypoxia or room air conditions. Overall design: One replicate was generated for each histone mark in each condition for a total of 4 immunoprecipitated samples and no input or control sample.ENAfalseMus musculusEpigenetic profiling of aorta macrophages of mice exposed to intermittent hypoxia (CD11ME)2025-09-242017-06-14PRJNA342773GSE868511009028240319