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chr1_15989440_G_T

chr1:15989440 · GRCh38GTrs891278420receptor_confirmed

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

Receptor variant-effect scores

PXR
0.025Neutral
FXR
0.067Neutral
AhR
0.278GoF
-1 LoF0+1 GoF

Strongest effect: AhR GoF at p99-scaled 0.278. 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
0.35
dbSNP
rs891278420
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
GA0.0250.0670.272not observed
GC0.0310.0670.307not observed
GT0.0250.0670.278not observed

Every possible base substitution at chr1:15989440, 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