This gene encodes a member of the poly(ADP-ribose) polymerase (PARP) protein family. The encoded anti-apoptotic protein may regulate aerobic glycolysis and promote survival of cancer cells. Increased expression of this gene has been reported in a variety of tumor types. [provided by RefSeq, Jul 2016]
Transcription factors with Perturb-seq knockdown data for PARP14. The Binding column indicates whether any binding evidence exists for this TF–gene pair (ChIP-seq or motif footprint peaks). The Mean coef is the average Perturb-seq regression coefficient across active gRNAs (positive = PARP14 upregulated upon KD; negative = downregulated). The Outlier column indicates whether this gene is in the top or bottom 5% of all TF knockdown effects.
| TF | Mean coef | Binding | Outlier | TF→Gene link |
|---|
Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of PARP14, linked by TSS proximity or chromatin conformation (Multiome / HiCAR). Each element overlaps at least one TF ChIP-seq binding site — the TFs column shows how many distinct TFs bind that element.
| Accessibility | Element | Dist. to TSS | Link type | TFs |
|---|---|---|---|---|
| chr3:122,382,880–122,383,692 | 297.8 kb | Distal (>10kb) Multiome | 711 | |
| chr3:122,383,843–122,384,747 | 296.6 kb | Distal (>10kb) Multiome | 937 | |
| chr3:122,442,936–122,443,707 | 237.5 kb | Distal (>10kb) Multiome | 134 | |
| chr3:122,514,019–122,515,266 | 166.0 kb | Distal (>10kb) Multiome HiCAR | 888 | |
| chr3:122,564,086–122,564,854 | 116.4 kb | Distal (>10kb) Multiome | 849 | |
| chr3:122,679,167–122,679,828 | 1.0 kb | Proximal (<10kb) | 357 | |
| chr3:122,680,509–122,681,348 | 169 bp | At TSS Multiome | 567 | |
| chr3:122,798,643–122,799,856 | 118.4 kb | Distal (>10kb) Multiome | 131 | |
| chr3:122,890,181–122,890,667 | 209.5 kb | Distal (>10kb) Multiome | 154 | |
| chr3:122,942,761–122,943,436 | 262.3 kb | Distal (>10kb) Multiome | 336 | |
| chr3:122,975,104–122,975,992 | 294.7 kb | Distal (>10kb) Multiome | 338 |
Genomic view of the PARP14 locus showing ATAC-seq accessibility and RNA-seq expression across the ESC → DE time course, together with TF binding peaks and element-to-TSS loop connections.