Variant report
Variant | rs564704 |
---|---|
Chromosome Location | chr6:54334494-54334495 |
allele | A/C |
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 | chr6:54334351..54336130-chr6:54337919..54340373,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10807471 | 0.90[EUR][1000 genomes] |
rs10807472 | 0.90[EUR][1000 genomes] |
rs10948821 | 0.81[EUR][1000 genomes] |
rs12055676 | 0.90[EUR][1000 genomes] |
rs1477583 | 0.90[EUR][1000 genomes] |
rs1820408 | 0.90[EUR][1000 genomes] |
rs1834483 | 0.90[EUR][1000 genomes] |
rs1985174 | 0.81[EUR][1000 genomes] |
rs243772 | 0.82[ASN][1000 genomes] |
rs243773 | 0.82[ASN][1000 genomes] |
rs3864316 | 0.90[EUR][1000 genomes] |
rs4090740 | 0.90[EUR][1000 genomes] |
rs4280961 | 0.90[EUR][1000 genomes] |
rs4427000 | 0.90[EUR][1000 genomes] |
rs496285 | 1.00[EUR][1000 genomes] |
rs513780 | 1.00[EUR][1000 genomes] |
rs519386 | 0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs522159 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs530355 | 0.90[EUR][1000 genomes] |
rs547320 | 0.84[ASN][1000 genomes] |
rs558698 | 1.00[EUR][1000 genomes] |
rs569189 | 1.00[EUR][1000 genomes] |
rs57572567 | 0.90[EUR][1000 genomes] |
rs587128 | 1.00[EUR][1000 genomes] |
rs59094137 | 0.90[EUR][1000 genomes] |
rs615537 | 0.95[EUR][1000 genomes] |
rs634239 | 1.00[EUR][1000 genomes] |
rs638540 | 0.82[ASN][1000 genomes] |
rs661622 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs675064 | 1.00[EUR][1000 genomes] |
rs7742798 | 0.90[EUR][1000 genomes] |
rs7757433 | 0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs9349714 | 0.90[EUR][1000 genomes] |
rs9349716 | 0.90[EUR][1000 genomes] |
rs9357809 | 0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs9367576 | 0.90[EUR][1000 genomes] |
rs9367577 | 0.90[EUR][1000 genomes] |
rs9367578 | 0.90[EUR][1000 genomes] |
rs9370303 | 0.90[EUR][1000 genomes] |
rs9370304 | 0.90[EUR][1000 genomes] |
rs9370308 | 0.90[EUR][1000 genomes] |
rs9370311 | 0.90[EUR][1000 genomes] |
rs9382350 | 0.90[EUR][1000 genomes] |
rs9382352 | 0.83[EUR][1000 genomes] |
rs9382354 | 0.90[EUR][1000 genomes] |
rs9382355 | 0.90[EUR][1000 genomes] |
rs9382356 | 0.90[EUR][1000 genomes] |
rs9395966 | 0.90[EUR][1000 genomes] |
rs9395968 | 0.85[EUR][1000 genomes] |
rs9395973 | 0.90[EUR][1000 genomes] |
rs9474894 | 0.90[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1067663 | chr6:53796341-54449718 | Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
2 | nsv529158 | chr6:53796341-54449718 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
3 | nsv528901 | chr6:54290333-54337130 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv427757 | chr6:54296552-54507210 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv970682 | chr6:54325591-54375255 | Enhancers Weak transcription Strong transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:54328800-54338200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr6:54329000-54338200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |