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chr11_679709_C_T

chr11:679709 · GRCh38CTrs1474675826gnomAD AF 1.97e-5receptor_confirmed

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

Receptor variant-effect scores

PXR
0.147GoF
FXR
0.179GoF
AhR
0.199GoF
-1 (LoF)0+1 (GoF)

Strongest effect: AhR GoF at normalized 0.199. Impact is low, near neutral.

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 · record
phyloP conservation
7.01 · conserved
gnomAD
AF 1.97e-5 · browser
dbSNP
rs1474675826
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
CA0.0170.038-0.018not observed
CG0.1030.1280.193not observed
CT0.1470.1790.1992.0e-5

Every possible base substitution at chr11:679709, 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: FXR

Multi receptor overlap: FXR

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.