Home / Variant

chr9_37422356_A_C

chr9:37422356 · GRCh38ACreceptor_confirmed

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

Receptor variant-effect scores

PXR
-0.742LoF
FXR
-0.655LoF
AhR
-0.536LoF
-1 LoF0+1 GoF

Strongest effect: PXR LoF at p99-scaled -0.742. Impact is large relative to 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

phyloP conservation
0.26
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
AC-0.742-0.655-0.536not observed
AG-0.161-0.128-0.052not observed
AT-0.252-0.249-0.170not observed

Every possible base substitution at chr9:37422356, 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: AhR