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chr7_191988_G_C

chr7:191988 · GRCh38GCrs1785556247gnomAD AF 1.65e-4ATAC_only

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

Receptor variant-effect scores

PXR
0.103GoF
FXR
-0.034Neutral
AhR
0.297GoF
-1 (LoF)0+1 (GoF)

Strongest effect: AhR GoF at normalized 0.297. 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

No external database record for this variant. It is a scored in silico saturation SNV.

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
GA0.092-0.0070.4807.2e-6
GC0.103-0.0340.2971.7e-4
GT0.007-0.0590.1147.2e-6

Every possible base substitution at chr7:191988, 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: none

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.