Experiment / E8A40B7CAWhole-Genome STARR-seq (WHG-STARR-seq)

HepG2 nonmethylated genomic STARR-seq

Sequence determinants of human gene regulatory elements

Approximately 500-bp sheared human genomic fragments were assayed without exogenous CpG methylation in HepG2 cells using an episomal STARR-seq reporter. This table combines the source MACS2 narrowPeak calls from the two HepG2 biological 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; nonmethylated genomic library

Unbiased human genomic DNA fragments were cloned into the 3′ UTR of the pCpG-free-Sasaki-SS reporter and measured by STARR-seq in HepG2. The source is the hg19 GSE180152 narrowPeak output for HepG2 NM replicates 1 and 2; methylation was not applied to this library.

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 · 14 definitions
sample_accession
GEO sample accession
replicate
HepG2 replicate or source sample label
chrom
hg19 chromosome
start
Zero-based genomic start coordinate
end
Half-open genomic end coordinate
peak_name
Source peak identifier
score
Source BED/narrowPeak display score
strand
Source strand field
signal_value
MACS2 signal value
neg_log10_p_value
MACS2 -log10 nominal p-value
neg_log10_q_value
MACS2 -log10 q-value
summit_offset
Peak summit offset from start
summit_coordinate
Derived hg19 summit coordinate
peak_length
Derived peak length in bases

Quality control

The source peak files are the paper's MACS2/blacklist-filtered processed outputs. Package QC required integer hg19 coordinates with start < end, valid strands, and finite peak statistics; all 13,790 combined peaks passed and were retained with sample accession and replicate labels.

Curation notes

This experiment combines GSM5454437 (NM1) and GSM5454438 (NM2) while retaining their source labels. The table contains genomic activity peaks, not allele-specific variant effects.

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