Home / Variant

chr17_75182799_C_A

chr17:75182799 · GRCh38CArs941342804receptor_confirmed

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

Receptor variant-effect scores

PXR
0.023Neutral
FXR
0.064Neutral
AhR
0.506GoF
-1 LoF0+1 GoF

Strongest effect: AhR GoF at p99-scaled 0.506. 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

phyloP conservation
0.70
dbSNP
rs941342804
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
CA0.0230.0640.506not observed
CG-0.0460.0030.0670.0039%
CT0.0260.0540.393not observed

Every possible base substitution at chr17:75182799, 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