ENCODE Regulation Txn Fac ChIP V2 Track Settings
 
Transcription Factor ChIP-seq from ENCODE (V2)

Track collection: Integrated Regulation from ENCODE

-  Description

These tracks contain information relevant to the regulation of transcription from the ENCODE project. The Transcription track shows transcription levels assayed by sequencing of polyadenylated RNA from a variety of cell types. The Overlayed H3K4Me1 and Overlayed H3K27Ac tracks show where modification of histone proteins is suggestive of enhancer and, to a lesser extent, other regulatory activity. These histone modifications, particularly H3K4Me1, are quite broad. The actual enhancers are typically just a small portion of the area marked by these histone modifications. The Overlay H3K4Me3 track shows a histone mark associated with promoters. The DNase Clusters track shows regions where the chromatin is hypersensitive to cutting by the DNase enzyme, which has been assayed in a large number of cell types. Regulatory regions, in general, tend to be DNase sensitive, and promoters are particularly DNase sensitive. The Txn Factor ChIP tracks show DNA regions where transcription factors, proteins responsible for modulating gene transcription, bind as assayed by chromatin immunoprecipitation with antibodies specific to the transcription factor followed by sequencing of the precipitated DNA (ChIP-seq).

These tracks complement each other and together can shed much light on regulatory DNA. The histone marks are informative at a high level, but they have a resolution of just ~200 bases and do not provide much in the way of functional detail. The DNase hypersensitive assay is higher in resolution at the DNA level and can be done on a large number of cell types since it's just a single assay. At the functional level, DNase hypersensitivity suggests that a region is very likely to be regulatory in nature, but provides little information beyond that. The transcription factor ChIP assay has a high resolution at the DNA level, and, due to the very specific nature of the transcription factors, is often informative with respect to functional detail. However, since each transcription factor must be assayed separately, the information is only available for a limited number of transcription factors on a limited number of cell lines. Though each assay has its strengths and weaknesses, the fact that all of these assays are relatively independent of each other gives increased confidence when multiple tracks are suggesting a regulatory function for a region.

For additional information please click on the hyperlinks for the individual tracks above. Also note that additional histone marks and transcription information is available in other ENCODE tracks. This integrative Super-track just shows a selection of the most informative data of general interest.

To view the full description, click here.

-  All tracks in this collection (8)
Transcription Transcription Levels Assayed by RNA-seq on 9 Cell Lines from ENCODE
Layered H3K4Me1 H3K4Me1 Mark (Often Found Near Regulatory Elements) on 7 cell lines from ENCODE
Layered H3K4Me3 H3K4Me3 Mark (Often Found Near Promoters) on 7 cell lines from ENCODE
Layered H3K27Ac H3K27Ac Mark (Often Found Near Active Regulatory Elements) on 7 cell lines from ENCODE
DNase Clusters DNaseI Hypersensitivity Clusters in 125 cell types from ENCODE (V3)
Txn Factr ChIP E3 Transcription Factor ChIP-seq Clusters (338 factors, 130 cell types) from ENCODE 3
Txn Factor ChIP Transcription Factor ChIP-seq Clusters (161 factors) from ENCODE with Factorbook Motifs
Txn Fac ChIP V2 Transcription Factor ChIP-seq from ENCODE (V2)

Display mode:      Duplicate track

Cluster right label: cell count (detected/assayed)   cell abbreviations

+  Cell Abbreviations
Metadata:
Principal Investigator on grant:Kent
Lab producing data:Kent - UC Santa Cruz
Experiment (Assay) type:Integ Cluster
Date restrictions end:2011-10-21
tableName:wgEncodeRegTfbsClusteredV2
File Name for downloading:wgEncodeRegTfbsClusteredV2.bed.gz
Data schema/format description and download
Source data version: ENCODE Jan 2011 Freeze
Assembly: Human Feb. 2009 (GRCh37/hg19)
Data last updated at UCSC: 2019-01-10

Description

This track shows regions where transcription factors, proteins responsible for modulating gene transcription, bind to DNA as assayed by ChIP-seq (chromatin immunoprecipitation with antibodies specific to the transcription factor followed by sequencing of the precipitated DNA). Additional views of this dataset and additional documentation on the methods used for this track are available at the ENC TF Binding Supertrack page. The peaks were computed using a uniform pipeline developed by Anshul Kundaje that uses the variation between the two replicates to develop sensible peak thresholds. This track combines data from many different cell lines and transcription-factor targeting antibodies into a relatively dense display.

Display Conventions

A gray box encompasses the peaks of transcription factor occupancy. The darkness of the box is proportional to the maximum signal strength observed in any cell line. The name to the left of the box is the transcription factor. The letters to the right represent the cell lines where a signal is detected. The darkness of the letter is proportional to the signal strength in the cell line. Click on an item in the track to see the cell lines spelled out.

Release Notes

Release 2 (May 2012) of this track fixes a bug that, in some cases, was causing the score values of signals within a cluster to be displayed incorrectly.

Credits

This track shows data from the Myers Lab at the HudsonAlpha Institute for Biotechnology and by the labs of Michael Snyder, Mark Gerstein and Sherman Weissman at Yale University; Peggy Farnham at UC Davis; and Kevin Struhl at Harvard. Kevin White at The University of Chicago. Vishy Iyer at The University of Texas Austin.

Data Release Policy

Data users may freely use ENCODE data, but may not, without prior consent, submit publications that use an unpublished ENCODE dataset until nine months following the release of the dataset. The full data release policy for ENCODE is available here.