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chr22_50481614_C_T

chr22:50481614 · GRCh38CTrs1207309491receptor_confirmed

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

Receptor variant-effect scores

PXR
0.099Neutral
FXR
0.173GoF
AhR
1.000GoF
-1 (LoF)0+1 (GoF)

Strongest effect: AhR GoF at normalized 1.000. Impact is at or above the receptor peak population 99th percentile, the top 1% or so.

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
2.05 · conserved
dbSNP
rs1207309491
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
CA0.0850.1641.000not observed
CG0.0450.1080.904not observed
CT0.0990.1731.000not observed

Every possible base substitution at chr22:50481614, 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.