Home / Variant

chr9_113989502_C_T

chr9:113989502 · GRCh38CTrs569779162gnomAD AF 0.0066%receptor_confirmed

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

Receptor variant-effect scores

PXR
-0.641LoF
FXR
-0.604LoF
AhR
-0.497LoF
-1 LoF0+1 GoF

Strongest effect: PXR LoF at p99-scaled -0.641. 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
0.11
gnomAD
AF 0.0066%
dbSNP
rs569779162
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-0.157-0.182-0.170not observed
CG-0.070-0.115-0.039not observed
CT-0.641-0.604-0.4970.0066%

Every possible base substitution at chr9:113989502, 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: FXR