Home / Variant

chr1_16178825_A_G

chr1:16178825 · GRCh38AGrs1497406gnomAD AF 47.3%receptor_confirmed

Regulatory target EPHA2 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
-0.740LoF
FXR
-0.877LoF
AhR
-0.772LoF
-1 LoF0+1 GoF

Strongest effect: FXR LoF at p99-scaled -0.877. 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

GTEx liver eQTL
EPHA2, slope -0.40, p 2.0e-19
GWAS Catalog
Alanine aminotransferase levels
phyloP conservation
0.12
gnomAD
AF 47.3%
dbSNP
rs1497406
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-0.109-0.3400.000not observed
AG-0.740-0.877-0.77247.3%
AT-0.520-0.708-0.550not observed

Every possible base substitution at chr1:16178825, 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