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chr16_89686714_G_A
For a non-coding regulatory variant the nearest gene by distance is frequently not the regulated gene.
Receptor variant-effect scores
Strongest effect: AhR GoF at normalized 0.202. Impact is moderate.
ft_head_delta_norm = center bin sum of ALT minus REF on the receptor CHIP_TF head, normalized to the peak population 99th percentile and clipped to [−1, 1]. AhR is reported as exploratory, single replicate.
Cross-annotations
- ClinVar
- Uncertain significance · Inborn genetic diseases · record
- phyloP conservation
- 0.28
- gnomAD
- AF 1.18e-4 · browser
- dbSNP
- rs2060197876
- Region tier
- receptor_confirmed
Mirrored from ClinVar, GTEx, GWAS Catalog, JASPAR/FIMO, gnomAD and phyloP. See Databases.
All substitutions at this position
| Substitution | PXR | FXR | AhR | gnomAD AF |
|---|---|---|---|---|
| G→A | -0.072 | 0.106 | 0.202 | 1.2e-4 |
| G→C | -0.105 | 0.003 | 0.034 | not observed |
| G→T | -0.020 | 0.071 | 0.124 | 6.6e-6 |
Every possible base substitution at chr16:89686714, each scored independently. The gnomAD column shows which substitution is actually seen in the population versus in silico only. Region confidence is the same for every substitution at this position, so it is shown once in the section below.
Region confidence
In receptor peaks: AhR
Multi receptor overlap: AhR
Binding motif
Logo for the strongest scoring receptor, AhR. The highlighted column marks the approximate affected base within the response element. External browser: UCSC Genome Browser.