<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE313nnn/GSE313891/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Methylation profiling</omics_type><species>Homo sapiens</species><gds_type>Methylation profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE313891</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Genome-wide methylation analysis defines the epigenetic identity of human innate lymphoid cells</name><description>DNA methylation of CpG motifs represents a stable epigenetic mark that critically influences the differentiation, stability and function of immune cell populations. Identifying differentially methylated regions within immune cell lineages contributes to their phenotypic and functional characterization, leading to a better understanding of lineage-specific transcriptional regulation. Here, we performed a genome-wide methylation analysis of human innate lymphoid cells (ILCs) isolated from tonsils and blood samples of healthy donors, which allowed us to define specific epigenetic marker regions for ILC1, ILC2 and ILC3.</description><dates><publication>2026/03/12</publication></dates><accession>GSE313891</accession><cross_references><GSM>GSM9377142</GSM><GSM>GSM9377153</GSM><GSM>GSM9377143</GSM><GSM>GSM9377144</GSM><GSM>GSM9377145</GSM><GSM>GSM9377150</GSM><GSM>GSM9377151</GSM><GSM>GSM9377152</GSM><GSM>GSM9377146</GSM><GSM>GSM9377147</GSM><GSM>GSM9377148</GSM><GSM>GSM9377149</GSM><GPL>24676</GPL><GSE>313891</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>