Enables protein-L-histidine N-tele-methyltransferase activity. Involved in actin modification and peptidyl-histidine methylation. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Transcription factors with Perturb-seq knockdown data for SETD3. 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 = SETD3 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 SETD3, 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 |
|---|---|---|---|---|
| chr14:99,230,631–99,232,582 | 248.8 kb | Distal (>10kb) Multiome | 274 | |
| chr14:99,245,498–99,247,127 | 234.9 kb | Distal (>10kb) Multiome | 314 | |
| chr14:99,262,920–99,263,579 | 217.8 kb | Distal (>10kb) Multiome | 160 | |
| chr14:99,270,416–99,271,381 | 210.1 kb | Distal (>10kb) Multiome | 301 | |
| chr14:99,271,901–99,274,036 | 207.5 kb | Distal (>10kb) Multiome | 584 | |
| chr14:99,274,138–99,275,258 | 206.1 kb | Distal (>10kb) Multiome | 708 | |
| chr14:99,479,847–99,482,007 | 289 bp | At TSS Multiome | 803 | |
| chr14:99,580,183–99,580,635 | 99.5 kb | Distal (>10kb) Multiome | 170 | |
| chr14:99,602,979–99,605,771 | 123.6 kb | Distal (>10kb) Multiome | 993 | |
| chr14:99,663,812–99,664,749 | 183.4 kb | Distal (>10kb) Multiome | 215 | |
| chr14:99,682,774–99,684,994 | 201.9 kb | Distal (>10kb) Multiome | 763 | |
| chr14:99,729,847–99,731,033 | 249.4 kb | Distal (>10kb) Multiome | 551 |
Genomic view of the SETD3 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.