<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>4D Nucleome Consortium</submitter><funding>NIDDK NIH HHS</funding><funding>NIDA NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NHGRI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pubmed_abstract>The dynamic three-dimensional (3D) organization of the human genome (the "4D Nucleome") is closely linked to genome function. Here, we integrate a wide variety of genomic data generated by the 4D Nucleome Project to provide a detailed view of human 3D genome organization in widely used embryonic stem cells (H1-hESCs) and immortalized fibroblasts (HFFc6). We provide extensive benchmarking of 3D genome mapping assays and integrate these diverse datasets to annotate spatial genomic features across scales. The data reveal a rich complexity of chromatin domains and their sub-nuclear positions, and over one hundred thousand structural loops and promoter-enhancer interactions. We developed 3D models of population-based and individual cell-to-cell variation in genome structure, establishing connec</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2024.09.17.613111</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11526861</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>An integrated view of the structure and function of the human 4D nucleome.</pubmed_title><pmcid>PMC11526861</pmcid><funding_grant_id>U54 DK107980</funding_grant_id><funding_grant_id>U01 DK127405</funding_grant_id><funding_grant_id>U01 CA200059</funding_grant_id><funding_grant_id>U54 DK107981</funding_grant_id><funding_grant_id>U01 CA200147</funding_grant_id><funding_grant_id>UM1 HG011593</funding_grant_id><funding_grant_id>U01 DA040612</funding_grant_id><funding_grant_id>U01 CA200060</funding_grant_id><funding_grant_id>UM1 HG011585</funding_grant_id><funding_grant_id>UM1 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Y</pubmed_authors><pubmed_authors>Boninsegna L</pubmed_authors><pubmed_authors>Janssens DH</pubmed_authors><pubmed_authors>Henikoff S</pubmed_authors><pubmed_authors>Pombo A</pubmed_authors><pubmed_authors>Zhao P</pubmed_authors><pubmed_authors>Veit A</pubmed_authors><pubmed_authors>Thieme CJ</pubmed_authors><pubmed_authors>Kempfer R</pubmed_authors><pubmed_authors>Emerson DJ</pubmed_authors><pubmed_authors>Schroeder A</pubmed_authors><pubmed_authors>Gehlenborg N</pubmed_authors><pubmed_authors>Alber F</pubmed_authors><pubmed_authors>Sengupta K</pubmed_authors><pubmed_authors>Phillips-Cremins JE</pubmed_authors><pubmed_authors>Kuang S</pubmed_authors><pubmed_authors>Peric-Hupkes D</pubmed_authors><pubmed_authors>Venev SV</pubmed_authors><pubmed_authors>Quinodoz SA</pubmed_authors><pubmed_authors>Chai H</pubmed_authors><pubmed_authors>Guttman M</pubmed_authors><pubmed_authors>Ren B</pubmed_authors><pubmed_authors>Marchal C</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Ehmsen S</pubmed_authors><pubmed_authors>Chilinski M</pubmed_authors><pubmed_authors>Ma J</pubmed_authors><pubmed_authors>Bakker C</pubmed_authors><pubmed_authors>Azcarate II</pubmed_authors><pubmed_authors>Ronchetti W</pubmed_authors><pubmed_authors>Chiariello AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>An integrated view of the structure and function of the human 4D nucleome.</name><description>The dynamic three-dimensional (3D) organization of the human genome (the "4D Nucleome") is closely linked to genome function. Here, we integrate a wide variety of genomic data generated by the 4D Nucleome Project to provide a detailed view of human 3D genome organization in widely used embryonic stem cells (H1-hESCs) and immortalized fibroblasts (HFFc6). We provide extensive benchmarking of 3D genome mapping assays and integrate these diverse datasets to annotate spatial genomic features across scales. The data reveal a rich complexity of chromatin domains and their sub-nuclear positions, and over one hundred thousand structural loops and promoter-enhancer interactions. We developed 3D models of population-based and individual cell-to-cell variation in genome structure, establishing connec</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2026-06-03T03:14:12.926Z</modification><creation>2025-04-19T04:26:19.865Z</creation></dates><accession>S-EPMC11526861</accession><cross_references><pubmed>39484446</pubmed><doi>10.1101/2024.09.17.613111</doi></cross_references></HashMap>