Variant report
Variant | rs11229511 |
---|---|
Chromosome Location | chr11:58283633-58283634 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10160259 | 1.00[AFR][1000 genomes] |
rs10160409 | 1.00[AFR][1000 genomes] |
rs10160825 | 1.00[AFR][1000 genomes] |
rs11229492 | 0.84[AFR][1000 genomes] |
rs11229507 | 1.00[AFR][1000 genomes] |
rs11229508 | 1.00[AFR][1000 genomes] |
rs11229523 | 1.00[AFR][1000 genomes] |
rs11229531 | 0.91[AFR][1000 genomes] |
rs11229546 | 1.00[AFR][1000 genomes] |
rs11229547 | 1.00[AFR][1000 genomes] |
rs11501583 | 1.00[AFR][1000 genomes] |
rs12271558 | 1.00[AFR][1000 genomes] |
rs12278835 | 0.84[AFR][1000 genomes] |
rs12282490 | 1.00[AFR][1000 genomes] |
rs12282535 | 1.00[AFR][1000 genomes] |
rs12282796 | 0.84[AFR][1000 genomes] |
rs12282872 | 1.00[AFR][1000 genomes] |
rs12282976 | 1.00[AFR][1000 genomes] |
rs12284057 | 1.00[AFR][1000 genomes] |
rs12286637 | 0.85[AFR][1000 genomes] |
rs12288841 | 1.00[AFR][1000 genomes] |
rs12290992 | 1.00[AFR][1000 genomes] |
rs12291718 | 0.91[AFR][1000 genomes] |
rs12293102 | 1.00[AFR][1000 genomes] |
rs12294453 | 1.00[AFR][1000 genomes] |
rs12294582 | 1.00[AFR][1000 genomes] |
rs28392851 | 0.84[AFR][1000 genomes] |
rs28543041 | 0.84[AFR][1000 genomes] |
rs28636578 | 1.00[AFR][1000 genomes] |
rs28853379 | 1.00[AFR][1000 genomes] |
rs35183671 | 0.84[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1054205 | chr11:57544264-58358509 | Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 67 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:58281800-58291400 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
2 | chr11:58281800-58291800 | Weak transcription | Muscle Satellite Cultured Cells | -- |