Home / Variant

chr17_77307122_C_T

chr17:77307122 · GRCh38CTrs372523373gnomAD AF 1.71e-4receptor_confirmed

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

Receptor variant-effect scores

PXR
0.662GoF
FXR
0.506GoF
AhR
0.551GoF
-1 (LoF)0+1 (GoF)

Strongest effect: PXR GoF at normalized 0.662. Impact is high, in the upper range toward the 99th percentile.

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

Disrupted motif
Rxra · JASPAR
phyloP conservation
0.75
gnomAD
AF 1.71e-4 · browser
dbSNP
rs372523373
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
CA1.0000.9620.888not observed
CG0.2540.0500.315not observed
CT0.6620.5060.5511.7e-4

Every possible base substitution at chr17:77307122, 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, PXR. The highlighted column marks the approximate affected base within the response element. External browser: UCSC Genome Browser.