Variant report
Variant | rs11847033 |
---|---|
Chromosome Location | chr14:64046484-64046485 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr11:62606585..62609127-chr14:64044498..64046630,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000133316 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10498511 | 0.87[EUR][1000 genomes] |
rs11158497 | 1.00[EUR][1000 genomes] |
rs11158504 | 0.82[EUR][1000 genomes] |
rs11845471 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs11845514 | 0.95[EUR][1000 genomes] |
rs11845765 | 0.82[EUR][1000 genomes] |
rs11846081 | 0.87[EUR][1000 genomes] |
rs11847188 | 0.87[EUR][1000 genomes] |
rs11847332 | 0.87[EUR][1000 genomes] |
rs11849082 | 0.82[EUR][1000 genomes] |
rs11850575 | 0.84[AMR][1000 genomes] |
rs11850853 | 0.91[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs12147764 | 0.91[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12147926 | 0.91[EUR][1000 genomes] |
rs17101346 | 0.87[EUR][1000 genomes] |
rs17101348 | 0.87[EUR][1000 genomes] |
rs17101355 | 0.87[EUR][1000 genomes] |
rs17101371 | 0.87[EUR][1000 genomes] |
rs3742622 | 0.87[EUR][1000 genomes] |
rs55665448 | 0.87[EUR][1000 genomes] |
rs55683626 | 1.00[AMR][1000 genomes] |
rs55706628 | 0.87[EUR][1000 genomes] |
rs55758170 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs55763522 | 0.91[EUR][1000 genomes] |
rs55797516 | 0.87[EUR][1000 genomes] |
rs55874427 | 0.87[EUR][1000 genomes] |
rs55919053 | 0.91[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs56015314 | 0.91[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs56021364 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs56051693 | 0.91[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs56060943 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs56094435 | 0.87[EUR][1000 genomes] |
rs56105514 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs56113838 | 0.87[EUR][1000 genomes] |
rs56169803 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs56247501 | 0.87[EUR][1000 genomes] |
rs56280069 | 0.91[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs56301550 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs56342043 | 0.87[EUR][1000 genomes] |
rs56388534 | 0.91[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs56858295 | 0.87[EUR][1000 genomes] |
rs56973820 | 0.87[EUR][1000 genomes] |
rs59420981 | 1.00[EUR][1000 genomes] |
rs61692440 | 0.91[EUR][1000 genomes] |
rs61984009 | 0.91[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs61984029 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs61984031 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs61984033 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs61984036 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs61984044 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs61984045 | 1.00[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs61984046 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs61984048 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs61984051 | 0.91[EUR][1000 genomes] |
rs61984055 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs61985669 | 0.87[EUR][1000 genomes] |
rs61985670 | 0.87[EUR][1000 genomes] |
rs61985671 | 0.87[EUR][1000 genomes] |
rs61985672 | 0.87[EUR][1000 genomes] |
rs61985674 | 0.83[EUR][1000 genomes] |
rs61985677 | 0.87[EUR][1000 genomes] |
rs61985680 | 0.87[EUR][1000 genomes] |
rs61985681 | 0.87[EUR][1000 genomes] |
rs61985682 | 0.87[EUR][1000 genomes] |
rs61985687 | 0.87[EUR][1000 genomes] |
rs61985689 | 0.87[EUR][1000 genomes] |
rs61985690 | 0.87[EUR][1000 genomes] |
rs61985691 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs6573528 | 0.87[EUR][1000 genomes] |
rs6573529 | 0.87[EUR][1000 genomes] |
rs7141460 | 0.87[EUR][1000 genomes] |
rs7142737 | 0.87[EUR][1000 genomes] |
rs7148755 | 0.87[EUR][1000 genomes] |
rs7149625 | 0.87[EUR][1000 genomes] |
rs7154718 | 0.87[EUR][1000 genomes] |
rs7154883 | 0.87[EUR][1000 genomes] |
rs7155351 | 0.87[EUR][1000 genomes] |
rs7156468 | 0.87[EUR][1000 genomes] |
rs73263634 | 0.87[EUR][1000 genomes] |
rs73263671 | 0.87[EUR][1000 genomes] |
rs73263676 | 0.91[EUR][1000 genomes] |
rs73265705 | 0.87[EUR][1000 genomes] |
rs73265719 | 0.82[EUR][1000 genomes] |
rs73265743 | 0.82[EUR][1000 genomes] |
rs8003101 | 0.87[EUR][1000 genomes] |
rs8003314 | 0.87[EUR][1000 genomes] |
rs8010642 | 0.87[EUR][1000 genomes] |
rs8013242 | 0.87[EUR][1000 genomes] |
rs8017282 | 0.91[EUR][1000 genomes] |
rs8017835 | 0.87[EUR][1000 genomes] |
rs8018194 | 0.83[EUR][1000 genomes] |
rs8018382 | 0.87[EUR][1000 genomes] |
rs8018872 | 0.87[EUR][1000 genomes] |
rs8019280 | 0.87[EUR][1000 genomes] |
rs8020833 | 0.87[EUR][1000 genomes] |
rs8020893 | 0.87[EUR][1000 genomes] |
rs9671362 | 0.87[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv527251 | chr14:63400786-64068806 | Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 28 gene(s) | inside rSNPs | diseases |
2 | nsv520528 | chr14:63400786-64157117 | Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 49 gene(s) | inside rSNPs | diseases |
3 | nsv915909 | chr14:63620440-64560369 | Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 67 gene(s) | inside rSNPs | diseases |
4 | nsv974442 | chr14:64024425-64046914 | Enhancers Weak transcription Bivalent Enhancer | TF binding regionChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:64045400-64050000 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
2 | chr14:64045600-64046600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
3 | chr14:64046400-64049600 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |