Home / Variant

chr8_143927204_T_C

chr8:143927204 · GRCh38TCrs11782890gnomAD AF 30.2%receptor_confirmed

Regulatory target PLEC 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
-0.732LoF
FXR
-0.816LoF
AhR
-1.000LoF
-1 LoF0+1 GoF

Strongest effect: AhR LoF at p99-scaled -1.000. Impact is at or beyond the receptor-specific p99 reference magnitude.

The p99-scaled score divides the raw delta by the receptor-specific 99th percentile of |delta| in the reference peak population, then clips to −1 to 1. It is a comparable effect scale, not a percentile rank. AhR is exploratory, from a single replicate.

Cross-annotations

ClinVar
Benign · not specified
GTEx liver eQTL
PLEC, slope -0.29, p 2.7e-9
phyloP conservation
-2.38
gnomAD
AF 30.2%
dbSNP
rs11782890
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-0.544-0.588-0.928not observed
TC-0.732-0.816-1.00030.2%
TG-0.320-0.300-0.588not observed

Every possible base substitution at chr8:143927204, each scored independently and shown as p99-scaled scores. 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: FXR