Home / Variant

chr15_63093708_A_C

chr15:63093708 · GRCh38ACrs186172356receptor_confirmed

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

Receptor variant-effect scores

PXR
-0.244LoF
FXR
-0.171LoF
AhR
-0.079Neutral
-1 LoF0+1 GoF

Strongest effect: PXR LoF at p99-scaled -0.244. 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

phyloP conservation
-1.96
dbSNP
rs186172356
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-0.244-0.171-0.079not observed
AG-0.0330.0450.177not observed
AT-0.241-0.131-0.1120.0099%

Every possible base substitution at chr15:63093708, 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