Variant report
Variant | rs11180914 |
---|---|
Chromosome Location | chr12:41819016-41819017 |
allele | A/G |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs11180888 | 1.00[CEU][hapmap];0.82[EUR][1000 genomes] |
rs11180898 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs11180905 | 1.00[CEU][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11180907 | 1.00[CEU][hapmap];0.91[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11180908 | 0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs11180912 | 1.00[CEU][hapmap];0.88[YRI][hapmap] |
rs12296173 | 0.91[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs12305552 | 1.00[CEU][hapmap];0.96[EUR][1000 genomes] |
rs12308926 | 1.00[CEU][hapmap];0.91[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12312032 | 1.00[CEU][hapmap];0.90[YRI][hapmap] |
rs12318761 | 0.82[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs12321550 | 0.91[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs12322196 | 1.00[CEU][hapmap];0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs285585 | 1.00[CEU][hapmap] |
rs4558215 | 1.00[CEU][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74077600 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74078808 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74078810 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs74078819 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs987823 | 1.00[CEU][hapmap];0.90[YRI][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv832383 | chr12:41693298-41846934 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | n/a |
2 | nsv832384 | chr12:41772648-41971430 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv899037 | chr12:41777144-41819215 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandlncRNA | 1 gene(s) | inside rSNPs | n/a |
4 | esv2755020 | chr12:41780758-41820936 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandlncRNA | 1 gene(s) | inside rSNPs | n/a |
5 | nsv899038 | chr12:41784137-41819215 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandlncRNA | 1 gene(s) | inside rSNPs | n/a |
6 | nsv1037987 | chr12:41815867-41840251 | Enhancers Weak transcription Active TSS Flanking Active TSS | TF binding regionCpG island | 1 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:41818000-41820600 | Enhancers | Pancreatic Islets | Pancreatic Islet |