Home / Variant

chr16_75251266_A_C

chr16:75251266 · GRCh38ACrs2151462057gnomAD AF 8.62e-1receptor_confirmed

Regulatory target ENSG00000280152 is taken from a GTEx liver eQTL, not from distance. For a non-coding regulatory variant the nearest gene by distance is frequently not the regulated gene.

Receptor variant-effect scores

PXR
-0.036Neutral
FXR
-0.104LoF
AhR
-0.770LoF
-1 (LoF)0+1 (GoF)

Strongest effect: AhR LoF at normalized -0.770. Impact is high, in the upper range toward the 99th percentile.

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

GTEx liver eQTL
ENSG00000280152, slope 0.48, p 1.8e-8
phyloP conservation
0.40
gnomAD
AF 8.62e-1 · browser
dbSNP
rs2151462057
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
AC-0.036-0.104-0.7708.6e-1
AG0.010-0.098-0.553not observed
AT0.036-0.028-0.045not observed

Every possible base substitution at chr16:75251266, 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.