Home / Variant

chr11_63974635_C_T

chr11:63974635 · GRCh38CTrs766632161gnomAD AF <0.001%receptor_confirmed

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

Receptor variant-effect scores

PXR
-0.301LoF
FXR
-0.358LoF
AhR
-0.749LoF
-1 LoF0+1 GoF

Strongest effect: AhR LoF at p99-scaled -0.749. 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
3.21 · conserved
gnomAD
AF <0.001%
dbSNP
rs766632161
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
CA-0.273-0.368-0.749not observed
CG-0.243-0.401-0.678<0.001%
CT-0.301-0.358-0.749<0.001%

Every possible base substitution at chr11:63974635, 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