Variant report
Variant | rs1472916 |
---|---|
Chromosome Location | chr5:108048835-108048836 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
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Variant related genes | Relation type |
---|---|
ENSG00000272523 | Chromatin interaction |
ENSG00000151422 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10079165 | 0.83[ASW][hapmap] |
rs1109617 | 1.00[CEU][hapmap];0.84[GIH][hapmap];0.95[MEX][hapmap];0.89[TSI][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs11240982 | 0.96[CEU][hapmap];0.81[EUR][1000 genomes] |
rs11739006 | 1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs12153703 | 0.96[CEU][hapmap];0.81[EUR][1000 genomes] |
rs13173714 | 1.00[CEU][hapmap];0.87[GIH][hapmap];0.95[MEX][hapmap];0.89[TSI][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs34660781 | 0.86[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs4957789 | 1.00[CEU][hapmap];0.95[GIH][hapmap];0.95[MEX][hapmap];0.89[TSI][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs6871143 | 0.85[CEU][hapmap] |
rs6871239 | 0.96[CEU][hapmap];0.84[GIH][hapmap];0.91[MEX][hapmap];0.81[EUR][1000 genomes] |
rs6889967 | 0.85[CEU][hapmap] |
rs6892439 | 0.81[EUR][1000 genomes] |
rs7700630 | 0.91[ASW][hapmap];0.81[MEX][hapmap] |
rs7716485 | 0.81[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv882689 | chr5:107595383-108299744 | Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 61 gene(s) | inside rSNPs | diseases |
No data |