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chr1_1158268_T_C
chr1:1158268 · GRCh38T → CgnomAD AF 0.0013%ATAC_only
For a non-coding regulatory variant the nearest gene by distance is frequently not the regulated gene.
Receptor variant-effect scores
PXR
-0.012small predicted occupancy change
FXR
0.096small predicted occupancy change
AhR
0.471predicted occupancy increase
-1 decrease0+1 increase
Strongest effect: AhR predicted occupancy increase at p99-scaled 0.471. 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
No external database record for this variant. It is a scored in silico saturation SNV.
Mirrored from ClinVar, GTEx, GWAS Catalog, JASPAR/FIMO, gnomAD and phyloP. See Databases.
Region confidence
In receptor peaks: none