Variant report
Variant | rs11828674 |
---|---|
Chromosome Location | chr11:84940166-84940167 |
allele | G/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 |
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rs_ID | r2[population] |
---|---|
rs11821196 | 0.90[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs11822075 | 0.83[AMR][1000 genomes] |
rs11822292 | 1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs11823950 | 0.83[AMR][1000 genomes] |
rs11824142 | 0.83[AMR][1000 genomes] |
rs11825860 | 1.00[YRI][hapmap];0.83[AMR][1000 genomes] |
rs11827460 | 0.83[AMR][1000 genomes] |
rs11828495 | 0.83[AMR][1000 genomes] |
rs11828752 | 0.83[AMR][1000 genomes] |
rs11829016 | 0.83[AMR][1000 genomes] |
rs55814754 | 0.90[AFR][1000 genomes] |
rs55893782 | 0.83[AMR][1000 genomes] |
rs55966246 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs57811920 | 0.83[AMR][1000 genomes] |
rs58960201 | 0.85[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs59597223 | 0.83[AMR][1000 genomes] |
rs59601533 | 0.83[AMR][1000 genomes] |
rs60507485 | 0.87[AFR][1000 genomes] |
rs60734054 | 0.83[AMR][1000 genomes] |
rs7111966 | 1.00[YRI][hapmap];0.80[AFR][1000 genomes] |
rs7926834 | 0.83[AMR][1000 genomes] |
rs7928064 | 1.00[YRI][hapmap];0.90[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1044370 | chr11:84748993-85293233 | Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 22 gene(s) | inside rSNPs | diseases |
2 | nsv898042 | chr11:84877221-84965437 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv898043 | chr11:84895033-85148689 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv898044 | chr11:84895033-85220773 | ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
No data |