Variant report
Variant | rs16920281 |
---|---|
Chromosome Location | chr11:94130485-94130486 |
allele | C/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 |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10466369 | 0.90[AMR][1000 genomes] |
rs11020824 | 0.81[LWK][hapmap];1.00[MEX][hapmap] |
rs11574858 | 0.81[LWK][hapmap] |
rs12284009 | 0.84[LWK][hapmap];1.00[MEX][hapmap] |
rs12294255 | 1.00[MEX][hapmap] |
rs13447578 | 1.00[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.88[YRI][hapmap];0.81[AFR][1000 genomes] |
rs13447593 | 0.88[AFR][1000 genomes] |
rs13447637 | 0.88[AFR][1000 genomes] |
rs13447693 | 0.86[AFR][1000 genomes] |
rs16920267 | 1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16920521 | 0.88[AFR][1000 genomes] |
rs58623923 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs58885207 | 0.80[AMR][1000 genomes] |
rs59895133 | 0.96[AFR][1000 genomes];0.90[AMR][1000 genomes] |
rs61734490 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7102892 | 0.88[AFR][1000 genomes] |
rs7102955 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7112263 | 0.88[YRI][hapmap];0.88[AFR][1000 genomes] |
rs7936320 | 1.00[MEX][hapmap] |
rs7937667 | 0.83[AFR][1000 genomes] |
rs7946384 | 1.00[MEX][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv523083 | chr11:93962121-94150790 | Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
2 | nsv832233 | chr11:93981434-94158471 | Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:94119600-94132400 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |