Variant report
Variant | rs2021277 |
---|---|
Chromosome Location | chr6:27163581-27163582 |
allele | A/C |
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:
1
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rs_ID | r2[population] |
---|---|
rs1102568 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11753248 | 1.00[ASN][1000 genomes] |
rs11753483 | 1.00[ASN][1000 genomes] |
rs11757216 | 1.00[ASN][1000 genomes] |
rs11965377 | 1.00[ASN][1000 genomes] |
rs11965529 | 0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11966985 | 1.00[ASN][1000 genomes] |
rs11967073 | 1.00[ASN][1000 genomes] |
rs11969536 | 1.00[ASN][1000 genomes] |
rs11970261 | 1.00[ASN][1000 genomes] |
rs16894325 | 1.00[AMR][1000 genomes] |
rs2893912 | 1.00[ASN][1000 genomes] |
rs34979454 | 1.00[ASN][1000 genomes] |
rs61745028 | 1.00[AMR][1000 genomes] |
rs73738797 | 1.00[ASN][1000 genomes] |
rs73740408 | 1.00[ASN][1000 genomes] |
rs858978 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs858979 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs858983 | 0.90[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948921 | chr6:26556890-27443957 | Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 472 gene(s) | inside rSNPs | diseases |
2 | esv3356749 | chr6:27155446-27163661 | Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats | Chromatin interactive region | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:27156800-27173000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |