<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/GSE345nnn/GSE345488/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Mus musculus</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE345488</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Allele-specific chromatin accessibility in early adolescence mouse liver resolved on a Collaborative Cross graph pangenome</name><description>To investigate the functional and adaptive significance of allele-specific candidate cis-regulatory elements (cCREs), we generated ATAC-seq on liver tissue from two 25-day-old F1 hybrid mice, bred from a CC032 mother and a CC072 father. Reads were mapped to the Collaborative Cross pangenome graph and phased into CC032 and CC072 alleles. Because no peak caller currently works directly on minigraph-cactus graphs, reads were surjected to GRCm38 for peak calling with MACS2. Counting phased reads on both alleles at 102,412 reproducible cCREs and testing for differential accessibility identified 1,805 allele-specific cCREs (1.7%) between the maternal and paternal genomes. About 72% of these carry SNVs and/or SVs from one allele, and they are enriched in promoters, introns and intergenic regions as well as in SINE, LINE and LTR transposable-element subfamilies.</description><dates><publication>2026/08/31</publication></dates><accession>GSE345488</accession><cross_references><GSM>GSM10005569</GSM><GSM>GSM10005568</GSM><GPL>24247</GPL><GSE>345488</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>