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chr22_21001871_T_G

chr22:21001871 · GRCh38TGrs1569161086gnomAD 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
-0.003Neutral
FXR
-0.078Neutral
AhR
-0.244LoF
-1 (LoF)0+1 (GoF)

Strongest effect: AhR LoF at normalized -0.244. 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

ClinVar
Uncertain significance · not specified · record
phyloP conservation
3.12 · conserved
gnomAD
AF 6.57e-6 · browser
dbSNP
rs1569161086
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-0.1030.1140.122not observed
TC0.0790.044-0.049not observed
TG-0.003-0.078-0.2446.6e-6

Every possible base substitution at chr22:21001871, 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.