SNP Report
Name | rs4987059 dbSNP Ensembl | ||
---|---|---|---|
Location | 11:636433 - 636433(+) | ||
Variant Seq | A | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.0421326 | ||
Annotation | upstream_gene_variant | ||
Variant Effect | upstream_gene_variant(ENST00000528733, ENST00000176183) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000176183) | ||
PolyPhen Annotation | unknown | ||
PolyPhen Variant Effect | unknown(ENST00000176183) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | TF binding region;Chromatin interactive region | ||
Chromatin State | Flanking Bivalent TSS/Enh;Bivalent Enhancer;Genic enhancers;Enhancers;Bivalent/Poised TSS;Strong transcription;Weak transcription | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature |