Home / Variant

chr2_111920393_G_T

chr2:111920393 · GRCh38GTrs867311receptor_confirmed

Regulatory target ENSG00000286904 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
-0.352LoF
FXR
-0.431LoF
AhR
-0.309LoF
-1 LoF0+1 GoF

Strongest effect: FXR LoF at p99-scaled -0.431. 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

GTEx liver eQTL
ENSG00000286904, slope -0.29, p 3.5e-6
phyloP conservation
-0.49
dbSNP
rs867311
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
GA-0.122-0.081-0.079not observed
GC-0.095-0.106-0.140not observed
GT-0.352-0.431-0.309not observed

Every possible base substitution at chr2:111920393, 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