Home / Variant

chr6_43267642_T_C

chr6:43267642 · GRCh38TCrs149936897receptor_confirmed

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

Receptor variant-effect scores

PXR
-0.091Neutral
FXR
-0.003Neutral
AhR
0.061Neutral
-1 LoF0+1 GoF

Strongest effect: PXR Neutral at p99-scaled -0.091. Impact is small on the receptor-specific p99 scale.

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

phyloP conservation
-1.69
dbSNP
rs149936897
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
TA0.002-0.003-0.024not observed
TC-0.091-0.0030.061not observed
TG0.0030.0030.024not observed

Every possible base substitution at chr6:43267642, 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: FXRAhR

Multi receptor overlap: FXR,AhR