Home / Variant

chr4_687353_A_C

chr4:687353 · GRCh38ACrs1741255360receptor_confirmed

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

Receptor variant-effect scores

PXR
-0.323LoF
FXR
-0.392LoF
AhR
-0.489LoF
-1 (LoF)0+1 (GoF)

Strongest effect: AhR LoF at normalized -0.489. 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
-0.43
dbSNP
rs1741255360
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-0.323-0.392-0.489not observed
AG-0.434-0.478-0.818not observed
AT-0.161-0.130-0.208not observed

Every possible base substitution at chr4:687353, 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: PXR

Multi receptor overlap: PXR

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.