Home / Variant

chr12_132398321_G_A

chr12:132398321 · GRCh38GArs1871604664receptor_confirmed

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

Receptor variant-effect scores

PXR
-0.012Neutral
FXR
-0.128LoF
AhR
-0.018Neutral
-1 (LoF)0+1 (GoF)

Strongest effect: FXR LoF at normalized -0.128. 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

Disrupted motif
Rxra · JASPAR
phyloP conservation
-0.82
dbSNP
rs1871604664
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
GA-0.012-0.128-0.018not observed
GC-0.017-0.1390.012not observed
GT-0.023-0.173-0.035not observed

Every possible base substitution at chr12:132398321, 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, FXR. The highlighted column marks the approximate affected base within the response element. External browser: UCSC Genome Browser.