Variant report
Variant | rs73516179 |
---|---|
Chromosome Location | chr9:96680155-96680156 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
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(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs56948438 | 1.00[AMR][1000 genomes] |
rs57233442 | 1.00[AMR][1000 genomes] |
rs58181103 | 1.00[AMR][1000 genomes] |
rs58459148 | 1.00[AMR][1000 genomes] |
rs58709329 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs59050355 | 1.00[AMR][1000 genomes] |
rs59264265 | 1.00[AMR][1000 genomes] |
rs59541311 | 1.00[AMR][1000 genomes] |
rs59630172 | 1.00[AMR][1000 genomes] |
rs60051875 | 1.00[AMR][1000 genomes] |
rs60230389 | 1.00[AMR][1000 genomes] |
rs60470247 | 1.00[AMR][1000 genomes] |
rs61384012 | 1.00[AMR][1000 genomes] |
rs73512601 | 1.00[AMR][1000 genomes] |
rs73514228 | 1.00[AMR][1000 genomes] |
rs73514235 | 1.00[AMR][1000 genomes] |
rs73514244 | 1.00[AMR][1000 genomes] |
rs73516177 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73516279 | 1.00[AMR][1000 genomes] |
rs73516289 | 1.00[AMR][1000 genomes] |
rs73516290 | 1.00[AMR][1000 genomes] |
rs73517142 | 1.00[AMR][1000 genomes] |
rs73517166 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73517183 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73517184 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73518259 | 1.00[AMR][1000 genomes] |
rs73518278 | 1.00[AMR][1000 genomes] |
rs73518291 | 1.00[AMR][1000 genomes] |
rs73519488 | 1.00[AMR][1000 genomes] |
rs73520278 | 1.00[AMR][1000 genomes] |
rs73520282 | 1.00[AMR][1000 genomes] |
rs73521324 | 1.00[AMR][1000 genomes] |
rs73521348 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73522141 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv893589 | chr9:96624645-96884544 | Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 18 gene(s) | inside rSNPs | diseases |
2 | nsv1053137 | chr9:96644876-96683214 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS | Chromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
3 | nsv1046904 | chr9:96647940-96689327 | Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh | Chromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
4 | nsv1035418 | chr9:96647940-96711409 | Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Active TSS Strong transcription | Chromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
5 | esv1801607 | chr9:96657324-96683214 | Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
6 | nsv1042043 | chr9:96657324-96689327 | Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | Chromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
7 | esv3356472 | chr9:96677831-96682029 | Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
8 | esv13498 | chr9:96679706-96680751 | Weak transcription Bivalent/Poised TSS Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:96677000-96685200 | Weak transcription | Spleen | Spleen |
2 | chr9:96679000-96682600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
3 | chr9:96679600-96680200 | Enhancers | Gastric | stomach |
4 | chr9:96679800-96680200 | Bivalent/Poised TSS | Breast Myoepithelial Primary Cells | Breast |
5 | chr9:96679800-96682400 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |