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chr9_117491629_A_G

chr9:117491629 · GRCh38AGrs1541155gnomAD AF 52.3%receptor_confirmed

Regulatory target ENSG00000233569 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
1.000GoF
FXR
1.000GoF
AhR
0.641GoF
-1 LoF0+1 GoF

Strongest effect: PXR GoF at p99-scaled 1.000. Impact is at or beyond the receptor-specific p99 reference magnitude.

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
ENSG00000233569, slope 0.27, p 1.0e-7
phyloP conservation
1.11
gnomAD
AF 52.3%
dbSNP
rs1541155
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
AC0.1200.0450.170not observed
AG1.0001.0000.64152.3%
AT0.1670.1660.039not observed

Every possible base substitution at chr9:117491629, 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