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chr22_21001902_G_T

chr22:21001902 · GRCh38GTrs1367921220receptor_confirmed

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

Receptor variant-effect scores

PXR
0.311GoF
FXR
-0.031Neutral
AhR
-0.318LoF
-1 (LoF)0+1 (GoF)

Strongest effect: AhR LoF at normalized -0.318. 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
6.47 · conserved
dbSNP
rs1367921220
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
GA0.294-0.104-0.440not observed
GC0.048-0.112-0.220not observed
GT0.311-0.031-0.318not observed

Every possible base substitution at chr22:21001902, 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, AhR. The highlighted column marks the approximate affected base within the response element. External browser: UCSC Genome Browser.