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chr9_17135031_C_A

chr9:17135031 · GRCh38CArs766825811receptor_confirmed

For a non-coding regulatory variant the nearest gene by distance is frequently not the regulated gene.

Receptor variant-effect scores

PXR
0.458GoF
FXR
0.348GoF
AhR
1.000GoF
-1 (LoF)0+1 (GoF)

Strongest effect: AhR GoF at normalized 1.000. Impact is at or above the receptor peak population 99th percentile, the top 1% or so.

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

phyloP conservation
1.66
dbSNP
rs766825811
Region tier
receptor_confirmed

Mirrored from ClinVar, GTEx, GWAS Catalog, JASPAR/FIMO, gnomAD and phyloP. See Databases.

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
CA0.4580.3481.000not observed
CG0.3010.2880.523not observed
CT-0.0820.1150.0261.3e-5

Every possible base substitution at chr9:17135031, 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: PXR

Multi receptor overlap: PXR

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.