Home / Variant

chr1_145425589_C_A

chr1:145425589 · GRCh38CArs1423146078receptor_confirmed

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

Receptor variant-effect scores

PXR
0.233GoF
FXR
0.063Neutral
AhR
0.211GoF
-1 LoF0+1 GoF

Strongest effect: PXR GoF at p99-scaled 0.233. 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

phyloP conservation
-1.12
dbSNP
rs1423146078
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
CA0.2330.0630.211not observed
CG0.2480.0910.292not observed
CT0.2150.0780.199not observed

Every possible base substitution at chr1:145425589, 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