Variant report
Variant | rs7111688 |
---|---|
Chromosome Location | chr11:84057482-84057483 |
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] |
---|---|
rs10160220 | 1.00[JPT][hapmap] |
rs10501561 | 0.91[CEU][hapmap];1.00[JPT][hapmap] |
rs10792757 | 1.00[JPT][hapmap] |
rs10898221 | 1.00[JPT][hapmap] |
rs10898229 | 1.00[CEU][hapmap];1.00[JPT][hapmap] |
rs10898230 | 1.00[JPT][hapmap] |
rs10898231 | 1.00[JPT][hapmap] |
rs10898233 | 1.00[JPT][hapmap] |
rs11233966 | 1.00[JPT][hapmap] |
rs11233969 | 1.00[JPT][hapmap] |
rs11234001 | 1.00[JPT][hapmap] |
rs11234010 | 0.82[EUR][1000 genomes] |
rs12274848 | 1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes] |
rs12277167 | 1.00[JPT][hapmap] |
rs12283368 | 1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.93[EUR][1000 genomes] |
rs12286690 | 1.00[JPT][hapmap] |
rs12360734 | 1.00[JPT][hapmap] |
rs1559855 | 1.00[JPT][hapmap] |
rs17147295 | 1.00[JPT][hapmap] |
rs7928075 | 1.00[JPT][hapmap] |
rs9651749 | 0.91[CEU][hapmap];1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948410 | chr11:83918339-84812001 | Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
2 | nsv1038641 | chr11:83996453-84334045 | Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv541103 | chr11:83996453-84334045 | Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv1049696 | chr11:84039547-84116297 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |