Variant report
Variant | rs11697525 |
---|---|
Chromosome Location | chr20:15511008-15511009 |
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)
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rs_ID | r2[population] |
---|---|
rs11697986 | 1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1362513 | 0.88[AFR][1000 genomes] |
rs6034213 | 0.87[CEU][hapmap] |
rs6043349 | 0.87[CEU][hapmap] |
rs6043350 | 0.86[CEU][hapmap] |
rs6043351 | 0.86[CEU][hapmap] |
rs6105428 | 0.93[CEU][hapmap];0.87[EUR][1000 genomes] |
rs6105432 | 1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.82[AMR][1000 genomes] |
rs6110663 | 0.81[CEU][hapmap] |
rs6110672 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs6110677 | 1.00[CEU][hapmap];0.89[EUR][1000 genomes] |
rs73098214 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73098216 | 0.89[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs73100235 | 0.97[AFR][1000 genomes];0.82[AMR][1000 genomes] |
rs73100236 | 0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9917445 | 0.86[CEU][hapmap] |
Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1062252 | chr20:14964258-15547739 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | nsv544206 | chr20:14964258-15547739 | Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | nsv869328 | chr20:15325423-16213898 | Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
4 | nsv833927 | chr20:15362602-15520185 | Enhancers Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | esv2751909 | chr20:15489871-15656007 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |