Home / Variant

chr19_44615969_T_C

chr19:44615969 · GRCh38TCrs1167778486receptor_confirmed

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

Receptor variant-effect scores

PXR
0.228GoF
FXR
0.340GoF
AhR
0.292GoF
-1 LoF0+1 GoF

Strongest effect: FXR GoF at p99-scaled 0.340. Impact is moderate 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
0.68
dbSNP
rs1167778486
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-0.013-0.057-0.042not observed
TC0.2280.3400.292not observed
TG-0.0030.0050.034not observed

Every possible base substitution at chr19:44615969, 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