Variant report
Variant | rs61755404 |
---|---|
Chromosome Location | chr7:126408729-126408730 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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(count:2 , 50 per page) page:
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Variant related genes | Relation type |
---|---|
ENSG00000179562 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11978791 | 0.92[AFR][1000 genomes] |
rs11981611 | 0.86[AFR][1000 genomes] |
rs11983585 | 0.95[AFR][1000 genomes] |
rs55774132 | 0.97[AFR][1000 genomes] |
rs56813278 | 0.92[AFR][1000 genomes] |
rs59577029 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6948817 | 0.86[AFR][1000 genomes] |
rs73720780 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73720781 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73720785 | 0.95[AFR][1000 genomes] |
rs73720798 | 0.88[AFR][1000 genomes] |
rs7778713 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7796521 | 1.00[AFR][1000 genomes] |

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 |