Variant report
Variant | rs12155429 |
---|---|
Chromosome Location | chr7:120408252-120408253 |
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 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10231690 | 0.87[EUR][1000 genomes] |
rs11976580 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs12154976 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs12673417 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs17132731 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs17142976 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs2189974 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs2525710 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs2721330 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs2721332 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs2721346 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs41622 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs41623 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs4281065 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4463360 | 0.99[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs4730982 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs6962226 | 0.83[EUR][1000 genomes] |
rs6978494 | 0.87[EUR][1000 genomes] |
rs73425852 | 0.99[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs73425856 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7805733 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs7810542 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs886440 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv1818826 | chr7:120405335-120622836 | Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:120407000-120414600 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |