MIR22HG
MIR22 host gene | DKFZp686O06159, MGC14376, C17orf91

Predicted to act upstream of or within response to wounding. Predicted to be part of RISC complex. [provided by Alliance of Genome Resources, Jul 2025]

Developmental clusters: GC7
Expression (TPM)
MIR22HG — as a Regulated Gene

TFs regulating MIR22HG 0 TFs

Transcription factors with Perturb-seq knockdown data for MIR22HG. 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 = MIR22HG upregulated upon KD; negative = downregulated). The Outlier column indicates whether this gene is in the top or bottom 5% of all TF knockdown effects.

Data: Effect:
TF Mean coef Binding Outlier TF→Gene link

Elements linked to MIR22HG

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of MIR22HG, 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
chr17:1,710,017–1,710,765 5.6 kb Proximal (<10kb) 500
chr17:1,713,886–1,717,908 at TSS At TSS 1042
chr17:1,724,373–1,725,206 8.0 kb Proximal (<10kb) 720

Genome Browser

Genomic view of the MIR22HG 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.

chr17:1,700,017 – 1,735,206
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq