Variant report
Variant | rs11649585 |
---|---|
Chromosome Location | chr16:79811605-79811606 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:4)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:4 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr16:79810413..79812648-chr16:79818258..79820940,2 | MCF-7 | breast: | |
2 | chr16:79810120..79812972-chr16:79839145..79841133,2 | MCF-7 | breast: | |
3 | chr16:79809357..79812774-chr16:79814579..79816705,4 | MCF-7 | breast: | |
4 | chr16:79802602..79806589-chr16:79809015..79812346,4 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000261390 | Chromatin interaction |
ENSG00000260876 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11150221 | 1.00[AFR][1000 genomes] |
rs11150222 | 1.00[AFR][1000 genomes] |
rs11639999 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs11643469 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12443838 | 0.91[EUR][1000 genomes] |
rs12444621 | 1.00[AFR][1000 genomes] |
rs4511553 | 1.00[ASN][1000 genomes] |
rs62041350 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62041351 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs62041353 | 1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs62041359 | 1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs62042360 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs62042363 | 1.00[ASN][1000 genomes] |
rs62042364 | 1.00[ASN][1000 genomes] |
rs62042365 | 1.00[ASN][1000 genomes] |
rs62042403 | 1.00[ASN][1000 genomes] |
rs62042404 | 1.00[ASN][1000 genomes] |
rs62042405 | 1.00[ASN][1000 genomes] |
rs62042408 | 1.00[ASN][1000 genomes] |
rs62042422 | 1.00[AFR][1000 genomes] |
rs62042423 | 1.00[AFR][1000 genomes] |
rs62042424 | 1.00[AFR][1000 genomes] |
rs62042429 | 1.00[AFR][1000 genomes] |
rs62042431 | 1.00[AFR][1000 genomes] |
rs7498926 | 0.87[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv573285 | chr16:79158182-80127326 | Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 28 gene(s) | inside rSNPs | diseases |
2 | nsv530714 | chr16:79661581-79925435 | Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
3 | nsv833296 | chr16:79692236-79889727 | Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
4 | nsv833297 | chr16:79732501-79920419 | Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
5 | esv2755409 | chr16:79776699-79816299 | Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:79810800-79817400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |