Variant report
Variant | rs9443847 |
---|---|
Chromosome Location | chr6:81615266-81615267 |
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] |
---|---|
rs12333152 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12333277 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1460186 | 1.00[AMR][1000 genomes] |
rs16892458 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16892604 | 1.00[EUR][1000 genomes] |
rs16892651 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4351211 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4351212 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4470815 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4543324 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55908144 | 1.00[EUR][1000 genomes] |
rs56790428 | 1.00[EUR][1000 genomes] |
rs6901453 | 1.00[EUR][1000 genomes] |
rs6915009 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6938275 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6940665 | 1.00[EUR][1000 genomes] |
rs73463365 | 1.00[EUR][1000 genomes] |
rs73471358 | 1.00[EUR][1000 genomes] |
rs7750118 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9443837 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9449173 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9449180 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9449181 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9449183 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531333 | chr6:81042427-81836484 | Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
2 | nsv886315 | chr6:81352515-81946866 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv886318 | chr6:81447367-81769538 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv1020546 | chr6:81536002-81616792 | Enhancers ZNF genes & repeats Weak transcription Active TSS | n/a | n/a | inside rSNPs | diseases |
5 | esv2763957 | chr6:81567637-81656379 | Enhancers ZNF genes & repeats Active TSS Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv1032130 | chr6:81572030-81722231 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | nsv1022379 | chr6:81585449-81621295 | Enhancers ZNF genes & repeats Weak transcription | n/a | n/a | inside rSNPs | diseases |
8 | nsv432936 | chr6:81588549-81632422 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | inside rSNPs | diseases |
9 | esv2762604 | chr6:81593275-81742093 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
10 | nsv516497 | chr6:81596450-81615591 | Enhancers Weak transcription ZNF genes & repeats | n/a | n/a | inside rSNPs | diseases |
11 | nsv428487 | chr6:81607405-81742838 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
12 | nsv830709 | chr6:81615127-81793247 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:81615000-81615400 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |