Variant report
Variant | rs6074881 |
---|---|
Chromosome Location | chr20:15341825-15341826 |
allele | G/T |
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] |
---|---|
rs1304180 | 1.00[ASN][1000 genomes] |
rs6043167 | 1.00[ASN][1000 genomes] |
rs6043172 | 1.00[ASN][1000 genomes] |
rs6043177 | 1.00[ASN][1000 genomes] |
rs6074873 | 1.00[ASN][1000 genomes] |
rs6074876 | 0.84[CEU][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6079725 | 1.00[ASN][1000 genomes] |
rs6079734 | 1.00[ASN][1000 genomes] |
rs6079736 | 1.00[ASN][1000 genomes] |
rs6079737 | 1.00[ASN][1000 genomes] |
rs6079739 | 1.00[ASN][1000 genomes] |
rs6079743 | 1.00[ASN][1000 genomes] |
rs6079745 | 1.00[ASN][1000 genomes] |
rs6079748 | 1.00[ASN][1000 genomes] |
rs6079751 | 1.00[ASN][1000 genomes] |
rs6079763 | 0.85[CEU][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6079764 | 0.91[CEU][hapmap];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6079765 | 0.85[CEU][hapmap];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6079771 | 0.92[CEU][hapmap];1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs6079773 | 1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6079780 | 1.00[CEU][hapmap] |
rs6079781 | 1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6079782 | 1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6079785 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6079786 | 0.83[EUR][1000 genomes] |
rs6079788 | 0.82[EUR][1000 genomes] |
rs7263594 | 1.00[ASN][1000 genomes] |
rs7353742 | 1.00[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1062252 | chr20:14964258-15547739 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | nsv544206 | chr20:14964258-15547739 | Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | nsv524481 | chr20:15007730-15382919 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
4 | nsv916795 | chr20:15041479-15345528 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
5 | nsv1058890 | chr20:15234769-15388360 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
6 | nsv912789 | chr20:15275538-15352001 | Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | nsv912790 | chr20:15317978-15352001 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
8 | nsv869328 | chr20:15325423-16213898 | Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
9 | nsv585630 | chr20:15335574-15360816 | Enhancers Weak transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr20:15327600-15346800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |