Variant report
Variant | rs12056229 |
---|---|
Chromosome Location | chr7:126371533-126371534 |
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 | chr7:126368803..126371577-chr7:126373352..126375062,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs12673913 | 0.83[CHB][hapmap];1.00[JPT][hapmap] |
rs12674061 | 0.82[JPT][hapmap];1.00[EUR][1000 genomes] |
rs2237770 | 0.82[JPT][hapmap];1.00[EUR][1000 genomes] |
rs2283077 | 0.82[JPT][hapmap];1.00[EUR][1000 genomes] |
rs2283078 | 0.82[JPT][hapmap];1.00[EUR][1000 genomes] |
rs2283080 | 0.82[JPT][hapmap];1.00[EUR][1000 genomes] |
rs2283081 | 1.00[EUR][1000 genomes] |
rs2299515 | 0.82[JPT][hapmap] |
rs3808163 | 0.84[CHB][hapmap];1.00[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv529300 | chr7:125669493-126587858 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
2 | nsv1032938 | chr7:126067684-126587859 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | nsv539119 | chr7:126067684-126587859 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
4 | nsv889187 | chr7:126219766-126478190 | Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer | Chromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
No data |