Home / Variant

chr18_63238336_G_T

chr18:63238336 · GRCh38GTrs1568242963receptor_confirmed

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

Receptor variant-effect scores

PXR
-0.121LoF
FXR
-0.151LoF
AhR
-0.444LoF
-1 (LoF)0+1 (GoF)

Strongest effect: AhR LoF at normalized -0.444. Impact is moderate.

ft_head_delta_norm = center bin sum of ALT minus REF on the receptor CHIP_TF head, normalized to the peak population 99th percentile and clipped to [−1, 1]. AhR is reported as exploratory, single replicate.

Cross-annotations

phyloP conservation
3.01 · conserved
dbSNP
rs1568242963
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-0.0460.005-0.006not observed
GC0.0310.0650.135not observed
GT-0.121-0.151-0.444not observed

Every possible base substitution at chr18:63238336, each scored independently. 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: FXR

Multi receptor overlap: FXR

Binding motif

Logo for the strongest scoring receptor, AhR. The highlighted column marks the approximate affected base within the response element. External browser: UCSC Genome Browser.