Experiment / E844ZNYQMEpisomal Plasmid MPRA

H3K27ac enhancer tiling library A

Analysis of long and short enhancers in melanoma cell states

A 190 bp tiling CHEQ-seq MPRA densely sampled H3K27ac-selected melanoma regions with overlapping tiles shifted by 20 bp. Library A includes wild-type tiles, motif-focused mutant tiles, and shuffled negative controls assayed across multiple melanoma cell-line replicates.

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

Basal / Untreated

CHEQ-seq 190 bp tile library with 20 bp shifts; library A included wild-type, motif-mutated, and shuffled sequences. Reporter activity was quantified by CPM-normalized cDNA/plasmid fold change across the replicate/cell-line columns supplied by GEO.

Processed data

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

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

Column dictionary · 21 definitions
element_id
Unique 190 bp tile identifier from the author processed table.
parent_region_id
Parent H3K27ac region inferred from the tile identifier before the tile suffix.
genomic_coordinates
hg19 tile coordinates parsed from the tile identifier.
tile_length_bp
Designed tile length in base pairs, generally 190 bp.
sequence_class
Author class for the tile: wt, mut, or shuffled.
variant_design
Mutation or design suffix supplied after the author’s tile delimiter; blank for unmodified tiles.
phenotype
Authors’ phenotype relationship annotation for the parent region.
mm029_rep1_activity_fc
CPM-normalized reporter cDNA/plasmid fold-change for MM029 replicate 1.
mm029_rep2_activity_fc
CPM-normalized reporter cDNA/plasmid fold-change for MM029 replicate 2.
mm057_rep1_activity_fc
CPM-normalized reporter cDNA/plasmid fold-change for MM057 replicate 1.
mm057_rep2_activity_fc
CPM-normalized reporter cDNA/plasmid fold-change for MM057 replicate 2.
mm074_rep2_activity_fc
CPM-normalized reporter cDNA/plasmid fold-change for MM074 replicate 2.
mm087_rep2_activity_fc
CPM-normalized reporter cDNA/plasmid fold-change for MM087 replicate 2.
mm087_rep3_activity_fc
CPM-normalized reporter cDNA/plasmid fold-change for MM087 replicate 3.
mm087_rep4_activity_fc
CPM-normalized reporter cDNA/plasmid fold-change for MM087 replicate 4.
mm099_rep1_activity_fc
CPM-normalized reporter cDNA/plasmid fold-change for MM099 replicate 1.
mm099_rep2_activity_fc
CPM-normalized reporter cDNA/plasmid fold-change for MM099 replicate 2.
n_measured_replicates
Number of finite activity measurements among the library-A replicate columns.
mean_activity_fc
Arithmetic mean of available tile activity fold changes; derived during packaging.
log2_mean_activity_fc
Base-2 logarithm of mean_activity_fc; derived during packaging.
qc_pass
TRUE for rows retained after removing all-missing tiles and applying source/agent QC.

Quality control

Author processing used Q>30 barcode reads, at least 5 barcodes per enhancer, plasmid-input normalization, shuffled controls/null modeling, and sample-level OutlierD/coverage filtering described in the paper. Rows with no finite activity in any replicate were removed (1,033 rows); valid partial measurements and wild-type, mutant, and shuffled controls were retained.

Curation notes

The source table contains 7,412 designed rows; 6,379 tiles with at least one finite activity value were retained. The three sequence classes and author-provided replicate columns are preserved, with missing replicate values left blank rather than imputed.

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