Home / Variant

chr12_124676090_C_A

chr12:124676090 · GRCh38CArs838503gnomAD AF 27.1%receptor_confirmed

Regulatory target ENSG00000280444 is taken from a GTEx liver eQTL, not from distance. For a non-coding regulatory variant the nearest gene by distance is frequently not the regulated gene.

Receptor variant-effect scores

PXR
0.023Neutral
FXR
-0.054Neutral
AhR
-0.246LoF
-1 LoF0+1 GoF

Strongest effect: AhR LoF at p99-scaled -0.246. Impact is moderate on the receptor-specific p99 scale.

The p99-scaled score divides the raw delta by the receptor-specific 99th percentile of |delta| in the reference peak population, then clips to −1 to 1. It is a comparable effect scale, not a percentile rank. AhR is exploratory, from a single replicate.

Cross-annotations

GTEx liver eQTL
ENSG00000280444, slope 0.31, p 8.9e-7
phyloP conservation
0.94
gnomAD
AF 27.1%
dbSNP
rs838503
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
CA0.023-0.054-0.24627.1%
CG0.022-0.058-0.251not observed
CT0.004-0.065-0.275<0.001%

Every possible base substitution at chr12:124676090, each scored independently and shown as p99-scaled scores. 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