Experiment / E1AGSTAL53' UTR / RNA Stability MPRA (MPRAu)

COSMIC somatic 3′-UTR variants in HeLa cells

Massively parallel screen uncovers many rare 3′ UTR variants regulating mRNA abundance of cancer driver genes

This library tested somatic 3′-UTR variants drawn from COSMIC and associated with cancer driver genes. Allele-specific mRNA abundance was measured with episomal MapUTR in HeLa cells.

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

Episomal pCAG-eGFP reporter assay using 200-nt reference/alternative oligos with a 164-nt tested 3′-UTR context. Plasmid DNA and poly(A)-selected reporter RNA were collected from three biological replicates approximately 24 h after electroporation; the author-provided MPRAnalyze statistics are retained alongside activity effects recomputed from deposited UMI counts.

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 · 48 definitions
variant_id
Stable identifier for the tested variant
chromosome
hg19 chromosome
position_hg19
1-based hg19 genomic coordinate
ref_allele
Reference allele tested
alt_allele
Alternative allele tested
gene
Host gene containing the tested 3′-UTR variant
gene_strand
Strand of the host gene
variant_group
Source variant collection (rare gnomAD/ExAC or COSMIC)
cell_line
Assayed cell line
chip_subpool
Oligo synthesis subpool identifier (for example, C1Sp1)
oligo_orientation
Design/sequencing orientation (orig or rc) when a deposited raw construct matched
published_result_qc_pass
True for rows present in the authors' all-tested result sheet after their upstream read, mapping, and UMI processing
author_functional_variant
Author's functional/non-functional call
effect_direction
Direction of the author's alternative/reference effect
author_lnfc_alt_vs_ref
Author-provided natural-log alternative/reference fold change from MPRAnalyze
author_activity_fold_change_alt_vs_ref
Exponential of the author lnFC, representing alternative/reference activity
author_activity_percent_change
100 times (author activity fold change minus 1)
author_p_value
Author-provided allelic test p-value
author_fdr
Author-provided multiple-testing-adjusted p-value
raw_count_complete
True when all 12 deposited DNA/RNA UMI count fields were available for both alleles
raw_count_min_10_qc
Diagnostic True when all 12 deposited DNA/RNA UMI counts were at least 10
raw_dna_total_umis
Sum of available deposited DNA UMI counts across both alleles and three replicates
raw_rna_total_umis
Sum of available deposited RNA UMI counts across both alleles and three replicates
dna_ref_rep1
Pre-transfection plasmid DNA UMI count for the reference allele, replicate 1
dna_ref_rep2
Pre-transfection plasmid DNA UMI count for the reference allele, replicate 2
dna_ref_rep3
Pre-transfection plasmid DNA UMI count for the reference allele, replicate 3
dna_alt_rep1
Pre-transfection plasmid DNA UMI count for the alternative allele, replicate 1
dna_alt_rep2
Pre-transfection plasmid DNA UMI count for the alternative allele, replicate 2
dna_alt_rep3
Pre-transfection plasmid DNA UMI count for the alternative allele, replicate 3
rna_ref_rep1
Poly(A)-selected reporter RNA UMI count for the reference allele, replicate 1
rna_ref_rep2
Poly(A)-selected reporter RNA UMI count for the reference allele, replicate 2
rna_ref_rep3
Poly(A)-selected reporter RNA UMI count for the reference allele, replicate 3
rna_alt_rep1
Poly(A)-selected reporter RNA UMI count for the alternative allele, replicate 1
rna_alt_rep2
Poly(A)-selected reporter RNA UMI count for the alternative allele, replicate 2
rna_alt_rep3
Poly(A)-selected reporter RNA UMI count for the alternative allele, replicate 3
activity_ref_rep1
Reference RNA/DNA UMI ratio, replicate 1
activity_ref_rep2
Reference RNA/DNA UMI ratio, replicate 2
activity_ref_rep3
Reference RNA/DNA UMI ratio, replicate 3
activity_alt_rep1
Alternative RNA/DNA UMI ratio, replicate 1
activity_alt_rep2
Alternative RNA/DNA UMI ratio, replicate 2
activity_alt_rep3
Alternative RNA/DNA UMI ratio, replicate 3
raw_log2fc_rep1
Raw log2 alternative/reference activity ratio, replicate 1
raw_log2fc_rep2
Raw log2 alternative/reference activity ratio, replicate 2
raw_log2fc_rep3
Raw log2 alternative/reference activity ratio, replicate 3
raw_mean_log2fc_alt_vs_ref
Mean raw log2 alternative/reference activity ratio across available replicates
raw_activity_fold_change_alt_vs_ref
2 raised to the raw mean log2 activity ratio
raw_activity_percent_change
100 times (raw activity fold change minus 1)
source_result_sheet
Source worksheet in the author's supplementary all-tested result workbook

Quality control

The authors retained perfectly mapped reads or reads with one mismatch outside the designed SNP, removed PCR duplicates using 15-mer UMIs, quantified DNA and poly(A) RNA UMI counts, quantile-normalized across three biological replicates, and tested allelic differences with a two-sided MPRAnalyze likelihood-ratio test. Functional calls use FDR ≤0.10 and an absolute relative-activity effect of at least 10%. This table retains all 11929 rows in the published all-tested Sheet 5 result sheet. Deposited UMI counts join completely for 11929 rows; 0 author-reported result rows have blank raw-count fields because no matching construct is present in the compact GEO export. Of the matched rows, 11703 have all 12 UMI counts ≥10; this is reported diagnostically and does not override the authors' result/QC universe.

Curation notes

The paper's COSMIC MapUTR library is deposited in GEO series GSE232572 with C4Sp1–C4Sp3 subpools. All 11,929 published result rows had a matching compact GEO UMI record; rows below the all-counts ≥10 diagnostic threshold remain because the authors' upstream pipeline and published all-tested result sheet are authoritative. Prime-editing follow-up experiments are not included because they are not MPRA data.

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