Created by Jessica Johnson
BOCA: Brain Open Chromatin Atlas
We have characterized the open chromatin by ATAC-seq assay in 14 brain regions and 2 cell types from 5 postmortem human brains.
Page content
Page content
- Abstract and link to the corresponding journal article
- Data accessions and links to GEO database and UCSC genome browser
- Interactive data visualisation of multidimensional scaling of samples groupped by brain regions and cell types
Abstract
Within each cell, specific patterns of open chromatin expose the cis regulatory elements required for proper spatiotemporal regulation of gene expression. To further understand the complex mechanisms that modulate gene expression in the human brain, we generated maps of neuronal and non-neuronal chromatin accessibility across 14 distinct brain regions of 5 adult individuals. Chromatin structure varies markedly by cell type and, across the brain, the most extensive differences are seen between neurons of the cortical regions, hippocampus, thalamus, and striatum. Differentially accessible chromatin overlaps with neuropsychiatric trait variants and identifies differences in molecular pathways and biological functions. Transcription factor footprinting and regulatory divergence analyses identify protein coding and long noncoding RNA with cell type and brain region specificity. Overall, these findings emphasize the importance of conducting cell-type and region-specific epigenetic studies to elucidate regulatory and disease-associated mechanisms in the human brain.
Data: UCSC hub
You can view the open chromatin tracks in the UCSC genome browser as a track hub by clicking this link:
Data: Downloads and individual tracks
You can view or download the individual files as individual tracks by following the links below. Be aware that the downloadable files are large (approximately 30GB in total). You can also access the GEO page for access to the individual sample data here or download BED files with region- & cell-type specific peaks (hg19, hg38), consensus peaks (hg19 hg38), raw count matrix (here), and normalized count matrix (here).Brain region | Bigwig hg19 | Bigwig hg38 | Sample | ||||||||||||||||
Broad area | name | abbreviation | neuronal | non-Neuronal | neuronal | non-Neuronal | 351 | 372 | 437 | 440 | 446 | ||||||||
Neocortex (NCX) | Dorsolateral prefrontal cortex | DLPFC |
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Orbitofrontal cortex | OFC |
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Ventrolatelar prefrontal cortex | VLPFC |
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Anterior cingulate cortex | ACC |
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Superior temporal cortex | STC |
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Inferior temporal cortex | ITC |
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Primary motor cortex | PMC |
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Insula | INS |
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Primary visual cortex | Primary visual cortex | PVC |
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Amygdala (AMY) | Amygdala | AMY |
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Hippocampus (HIP) | Hippocampus | HIP |
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Mediodorsal thalamus (MDT) | Mediodorsal thalamus | MDT |
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Striatum (STR) | Nucleus accumbens | NAC |
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Putamen | PUT |
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Interactive data visualisation
Multidimensional scaling of brain regions and cell types (n=28) using the pi1 estimates of statistical dissimilarity as distance (same abbreviations as in the above table are used). The MDT (mediodorsal thalamus) non-neuronal group is immediately adjacent to, and partly obscured by, the leftmost non-neuronal STR group (putamen). Move cursor over the data points to see full description.
© 2018 Roussos Lab at Icahn School of Medicine at Mount Sinai