Home / Variant

chr7_138890914_C_T

chr7:138890914 · GRCh38CTrs898174371receptor_confirmed

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

Receptor variant-effect scores

PXR
-0.060Neutral
FXR
-0.291LoF
AhR
-0.131LoF
-1 (LoF)0+1 (GoF)

Strongest effect: FXR LoF at normalized -0.291. 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
-1.73
dbSNP
rs898174371
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
CA-0.398-0.636-0.471not observed
CG-0.225-0.428-0.137not observed
CT-0.060-0.291-0.131not observed

Every possible base substitution at chr7:138890914, 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: AhR

Multi receptor overlap: AhR

Binding motif

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