HepG2 nonmethylated genomic STARR-seq
Sequence determinants of human gene regulatory elementsApproximately 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
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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.