Experiment / E769G8PA5Standard STARR-seq

Genome-scale GR ChIP-enriched STARR-seq reporter assay

Direct GR Binding Sites Potentiate Clusters of TF Binding across the Human Genome

A549 cells were transfected with an episomal STARR-seq library made from GR ChIP-seq fragments and treated with 100 nM dexamethasone or 0.02% ethanol vehicle for 3 h. The table contains the site-level DESeq2 reporter-RNA contrast for the 10,963 GR binding-site subpeaks that passed the publication's statistical-power filter.

Processed tables are specific to each experiment. Column names, units, measurements, and table structure are not standardized across the database. Check this experiment’s column definitions and quality-control notes before comparing or combining data.

Perturbation & assay details

100 nM dexamethasone for 3 h vs 0.02% ethanol vehicle control

GR ChIP-seq libraries were adapted and cloned into the 3' UTR of the GFP STARR-seq reporter backbone, transfected into A549 cells, and quantified from reporter RNA in three DEX and three ethanol biological replicate libraries. The published site-level statistics are DESeq2 normalized-count results for the DEX-versus-ethanol comparison.

Processed data

50 rows per page. Click a cell to inspect its full value.

Visible columns (17 of 17)
Row
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50

Filters apply to this table only. The CSV download contains the complete processed table; filtered rows are available through the API.

Column dictionary · 17 definitions
element_id
Published GR subpeak location identifier
location
Original Table S2 location string in the form chromosome_start_end
chromosome
Human chromosome from Location
start
Start of the one-base published subpeak-center interval
end
End of the one-base published subpeak-center interval
peak_center
Published subpeak-center coordinate, equal to start
chip_peak_start
Start of the corresponding 500-bp GR ChIP-seq peak from Table S1
chip_peak_end
End of the corresponding 500-bp GR ChIP-seq peak from Table S1
chip_merged_reads_per_peak
Merged GR ChIP-seq reads for the corresponding Table S1 peak
base_mean
DESeq2 mean normalized count across the reporter libraries
log2_fold_change_dex_vs_etoh
DESeq2 log2 fold change in reporter signal for DEX relative to ethanol
lfc_se
Standard error of the DESeq2 log2 fold-change estimate
wald_stat
DESeq2 Wald test statistic
pvalue
DESeq2 p-value for the DEX-versus-ethanol reporter contrast
padj
DESeq2 multiple-testing-adjusted p-value
response_class
Induced or repressed when padj < 0.05 and log2 fold change has the matching sign; otherwise not_significant
qc_pass
True for rows retained after the documented coordinate and numeric-statistic QC

Quality control

The source Table S2 contains 27,432 called GR subpeaks; 10,963 rows with numeric baseMean, log2FoldChange, lfcSE, statistic, p-value, and adjusted p-value were retained, matching the paper's stated sufficient-statistical-power filter. Each retained Location was required to map to a Table S1 500-bp peak centered at Location start; all 10,963 rows passed this coordinate check. No additional effect-size or FDR threshold was applied, so both significant and non-significant assayed sites remain in the table.

Curation notes

This is the primary genome-scale ChIP-reporter experiment, not the endogenous RNA-seq subseries. Location denotes the center of a fixed 500-bp GR ChIP-seq subpeak; it is not a variant identifier. The table intentionally retains the 9,587 source-assayed sites that were powered but not FDR-significant alongside 1,330 induced and 46 repressed sites. A549 resolves to Cellosaurus CVCL:0023.

Cite OpenMPRA

Cite the OpenMPRA database. Include your access date because the collection changes over time.

Please also cite the source studies when using their data.