Reference tracks plus IGVF/ENCODE browser files when available.
Region summary
Normalized coordinates: chr10:79286500-79287000
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Regulatory annotations, enhancer predictions, and functional measurements overlapping this region.
Which enhancers overlap this region, and what are their target genes and cell types? ENCODE-rE2G and scE2G models.
Which regulatory elements in this region have measured perturbation effects on gene expression (Perturb-seq, CRISPR screen)?
Reference-allele log2 fold change measurements for genomic elements overlapping this region. Alternative-allele assay results are available in portal downloads.
Which variants in this region (up to 10 kb) change regulatory activity in reporter assays (MPRA, STARR-seq) or are predicted to by BlueSTARR?
Variants within this region linked to genomic elements by chromatin accessibility QTLs (caQTL).
Variant evidence counts across methods for this region.
Total catalog variants overlapping this region, with counts grouped by evidence method.
Molecular QTL associations for variants overlapping this region.
Gene, protein, splice, and chromatin-accessibility QTL associations for variants overlapping this region.
Observed and predicted allele-specific binding evidence for variants overlapping this region.
Observed and predicted transcription factor binding effects for variants overlapping this region, including ADASTRA, GVATdb, and SEMVAR rows when available.
Phenotype associations for variants overlapping this region.
GWAS and other phenotype associations for variants overlapping this region.