Variant report
Variant | rs6676591 |
---|---|
Chromosome Location | chr1:75978010-75978011 |
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] |
---|---|
rs10158990 | 0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs10874314 | 0.82[CHB][hapmap];0.94[YRI][hapmap] |
rs11163435 | 0.85[JPT][hapmap] |
rs1249780 | 0.85[JPT][hapmap] |
rs1249781 | 0.85[JPT][hapmap] |
rs1249785 | 0.85[JPT][hapmap] |
rs1249795 | 0.85[JPT][hapmap] |
rs1249811 | 0.82[JPT][hapmap] |
rs1249814 | 0.85[JPT][hapmap] |
rs1249815 | 0.82[JPT][hapmap] |
rs1249816 | 0.85[JPT][hapmap] |
rs1249822 | 0.85[JPT][hapmap] |
rs1249849 | 0.82[JPT][hapmap] |
rs1249850 | 0.85[JPT][hapmap] |
rs1614816 | 0.85[JPT][hapmap] |
rs1739902 | 0.96[CEU][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs1778456 | 0.85[JPT][hapmap] |
rs1867352 | 0.82[CHB][hapmap] |
rs1889037 | 0.82[CHB][hapmap] |
rs1913124 | 0.85[JPT][hapmap] |
rs2347218 | 0.82[JPT][hapmap] |
rs2587031 | 0.82[JPT][hapmap] |
rs2799050 | 0.82[JPT][hapmap] |
rs6658825 | 0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
rs6672579 | 0.85[JPT][hapmap] |
rs6691590 | 0.85[JPT][hapmap] |
rs920813 | 0.96[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv519329 | chr1:75830438-76358591 | Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 35 gene(s) | inside rSNPs | diseases |
2 | esv3445096 | chr1:75933216-76126980 | Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |