Home / Variant

chr2_231464938_G_C

chr2:231464938 · GRCh38GCrs989796099receptor_confirmed

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

Receptor variant-effect scores

PXR
-0.075Neutral
FXR
-0.086Neutral
AhR
-0.371LoF
-1 (LoF)0+1 (GoF)

Strongest effect: AhR LoF at normalized -0.371. 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

phyloP conservation
0.09
dbSNP
rs989796099
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
GA0.016-0.030-0.146not observed
GC-0.075-0.086-0.371not observed
GT0.051-0.048-0.236not observed

Every possible base substitution at chr2:231464938, 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.