Variant report
| Variant | rs71643451 |
|---|---|
| Chromosome Location | chr1:217404370-217404371 |
| allele | A/G |
| 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:
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| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr1:217398384..217401178-chr1:217402478..217405024,2 | MCF-7 | breast: |
| No data |
| No data |
| No data |
| No data |
rSNPs within LD-proxies of this variant (count:21)
| rs_ID | r2[population] |
|---|---|
| rs11117818 | 0.93[AMR][1000 genomes] |
| rs12026070 | 0.85[AMR][1000 genomes] |
| rs12026072 | 0.82[AMR][1000 genomes] |
| rs12027079 | 0.90[AMR][1000 genomes];0.85[ASN][1000 genomes] |
| rs12030946 | 0.90[AMR][1000 genomes];0.85[ASN][1000 genomes] |
| rs12032192 | 0.86[AMR][1000 genomes];0.88[ASN][1000 genomes] |
| rs12044340 | 0.96[AMR][1000 genomes] |
| rs12723203 | 0.82[AMR][1000 genomes];0.84[ASN][1000 genomes] |
| rs4332417 | 0.81[ASN][1000 genomes] |
| rs4504960 | 0.90[AMR][1000 genomes] |
| rs4846822 | 0.90[AMR][1000 genomes];0.82[ASN][1000 genomes] |
| rs4846825 | 0.90[AMR][1000 genomes] |
| rs71643452 | 0.85[AMR][1000 genomes] |
| rs71643453 | 0.85[AMR][1000 genomes] |
| rs72745316 | 0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.81[ASN][1000 genomes] |
| rs7516676 | 0.90[AMR][1000 genomes];0.85[ASN][1000 genomes] |
| rs7534753 | 0.90[AMR][1000 genomes];0.82[ASN][1000 genomes] |
| rs7535701 | 0.90[AMR][1000 genomes];0.85[ASN][1000 genomes] |
| rs7543133 | 0.84[AMR][1000 genomes];0.85[ASN][1000 genomes] |
| rs7543660 | 0.90[AMR][1000 genomes];0.82[ASN][1000 genomes] |
| rs7547261 | 0.90[AMR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page:
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| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv549207 | chr1:217333272-217455903 | Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
| 2 | nsv1003559 | chr1:217354095-217418732 | Enhancers Weak transcription | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
| 3 | esv2762164 | chr1:217389951-217742750 | Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
| 4 | esv3452693 | chr1:217404307-217404714 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:217402800-217405800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
