Variant report
Variant | rs11835913 |
---|---|
Chromosome Location | chr12:75061904-75061905 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:1)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:1 , 50 per page) page:
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No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | FOS | chr12:75061828-75062041 | MCF10A-Er-Src | breast: | n/a | n/a |
No data |
No data |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000188646 | TF binding region |
rs_ID | r2[population] |
---|---|
rs10506688 | 0.90[EUR][1000 genomes] |
rs11180146 | 1.00[EUR][1000 genomes] |
rs11180186 | 0.95[EUR][1000 genomes] |
rs11837536 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs12297382 | 0.95[EUR][1000 genomes] |
rs12302658 | 0.95[EUR][1000 genomes] |
rs12315155 | 1.00[CEU][hapmap];0.95[EUR][1000 genomes] |
rs12319938 | 0.95[EUR][1000 genomes] |
rs12321065 | 0.95[EUR][1000 genomes] |
rs1508157 | 0.90[EUR][1000 genomes] |
rs17114150 | 0.95[EUR][1000 genomes] |
rs17185333 | 0.95[EUR][1000 genomes] |
rs17789260 | 0.95[EUR][1000 genomes] |
rs2102409 | 1.00[EUR][1000 genomes] |
rs55723402 | 0.95[EUR][1000 genomes] |
rs55916036 | 0.85[EUR][1000 genomes] |
rs55928489 | 0.95[EUR][1000 genomes] |
rs55983122 | 0.90[EUR][1000 genomes] |
rs56263223 | 0.95[EUR][1000 genomes] |
rs60341073 | 0.95[EUR][1000 genomes] |
rs74107525 | 0.95[EUR][1000 genomes] |
rs74107526 | 0.95[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv899297 | chr12:75045728-75169675 | Enhancers Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv899298 | chr12:75045728-75173289 | Enhancers Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
3 | nsv427915 | chr12:75047293-75172692 | Enhancers Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:75061600-75062000 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
2 | chr12:75061600-75062000 | Enhancers | NH-A | brain |