Variant report
Variant | rs1603455 |
---|---|
Chromosome Location | chr7:146908570-146908571 |
allele | A/G |
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 |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10229762 | 1.00[JPT][hapmap] |
rs10500174 | 1.00[JPT][hapmap] |
rs10952677 | 1.00[JPT][hapmap] |
rs12111644 | 1.00[JPT][hapmap] |
rs12111864 | 1.00[JPT][hapmap] |
rs12112963 | 1.00[JPT][hapmap] |
rs12703882 | 1.00[CEU][hapmap] |
rs12703884 | 1.00[CEU][hapmap];0.84[EUR][1000 genomes] |
rs12703890 | 1.00[JPT][hapmap] |
rs13232077 | 1.00[CEU][hapmap] |
rs13241146 | 1.00[JPT][hapmap];0.80[EUR][1000 genomes] |
rs1525213 | 1.00[JPT][hapmap] |
rs1603453 | 1.00[JPT][hapmap] |
rs1603456 | 1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
rs17170328 | 0.82[CEU][hapmap] |
rs17170331 | 1.00[CEU][hapmap] |
rs17170336 | 0.82[CEU][hapmap] |
rs17170339 | 0.82[CEU][hapmap] |
rs17170368 | 1.00[CEU][hapmap];1.00[JPT][hapmap] |
rs17170370 | 1.00[CEU][hapmap] |
rs17170371 | 1.00[JPT][hapmap] |
rs17409131 | 1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap] |
rs35265883 | 0.84[EUR][1000 genomes] |
rs4726831 | 1.00[JPT][hapmap] |
rs6464791 | 1.00[JPT][hapmap] |
rs6943628 | 1.00[CEU][hapmap];1.00[JPT][hapmap] |
rs6977005 | 1.00[JPT][hapmap] |
rs71530773 | 0.84[EUR][1000 genomes] |
rs7777057 | 1.00[JPT][hapmap] |
rs7806237 | 1.00[CEU][hapmap];1.00[JPT][hapmap] |
rs987420 | 1.00[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv933033 | chr7:146720301-147081560 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv1033898 | chr7:146721499-147081768 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv931005 | chr7:146730472-147381257 | Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 7 gene(s) | inside rSNPs | diseases |
4 | nsv889395 | chr7:146848251-146969389 | Enhancers Active TSS Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
5 | nsv889396 | chr7:146854133-147035067 | Enhancers Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | nsv5996 | chr7:146905699-146950685 | Enhancers | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |