Home / Variant

chr9_113275629_T_A

chr9:113275629 · GRCh38TArs1239444464gnomAD AF 6.57e-6receptor_confirmed

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

Receptor variant-effect scores

PXR
-0.346LoF
FXR
-0.093Neutral
AhR
-0.105LoF
-1 (LoF)0+1 (GoF)

Strongest effect: PXR LoF at normalized -0.346. 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
-1.75
gnomAD
AF 6.57e-6 · browser
dbSNP
rs1239444464
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
TA-0.346-0.093-0.1056.6e-6
TC-0.167-0.1150.0396.6e-6
TG-0.0210.0190.052not observed

Every possible base substitution at chr9:113275629, 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, PXR. The highlighted column marks the approximate affected base within the response element. External browser: UCSC Genome Browser.