Home / Variant

chr17_19579537_A_G

chr17:19579537 · GRCh38AGrs1048107466receptor_confirmed

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

Receptor variant-effect scores

PXR
0.048Neutral
FXR
0.007Neutral
AhR
0.111GoF
-1 (LoF)0+1 (GoF)

Strongest effect: AhR GoF at normalized 0.111. Impact is low, near neutral.

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
-0.44
dbSNP
rs1048107466
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
AC0.007-0.012-0.044not observed
AG0.0480.0070.111not observed
AT0.000-0.002-0.0136.6e-6

Every possible base substitution at chr17:19579537, 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.