Region chr10:79286500-79287000

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4 tables

Genome Browser

hg38

Reference tracks plus IGVF/ENCODE browser files when available.

Region summary

Normalized coordinates: chr10:79286500-79287000

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Gene Regulation

Regulatory annotations, enhancer predictions, and functional measurements overlapping this region.

---Enhancer-Gene PredictionsView documentation about Enhancer-Gene Prediction

Which enhancers overlap this region, and what are their target genes and cell types? model.

Cell Type
Target Gene
Score
Enhancer Coordinates
Dataset
Source

---ENCODE candidate cis-regulatory elements

Does this region overlap from ENCODE? SCREEN

Chromosome
Start Position
End Position
Element ID
Annotation
Element Type

---Measured region activitiesView documentation about Measured region activities

Reference-allele log2 fold change measurements for genomic elements overlapping this region. Alternative-allele assay results are available in portal downloads.

Coordinates
Element Name
Element Type
Source Annotation
Biosample
Method

---Variant-Genomic Element LinksView documentation about Variant-Genomic Element Links

Variants within this region linked to genomic elements (e.g., , ).

Variant
Genomic Element
Element Type
Coordinates
Biosample
Method

Variant Summary

Variant evidence counts across methods for this region.

---Region Variant SummariesView documentation about Region Variant Summary

Total catalog variants overlapping this region, with counts grouped by evidence method.

Method
Variant Count

Allele-Specific Binding

Observed and predicted allele-specific binding evidence for variants overlapping this region.

---Allele-Specific Binding EvidencesView documentation about Allele-Specific Binding Evidence

Observed and predicted transcription factor binding effects for variants overlapping this region, including , , and rows when available.

Variant
Protein / Complex
Method
Class
Label
Motif

Phenotypes

Phenotype associations for variants overlapping this region.

---Region Phenotype AssociationsView documentation about Region Phenotype Associations

and other phenotype associations for variants overlapping this region.

Variant
Trait
Study ID
Study Source
P-value
Effect Size