Variant report
Variant | rs17695807 |
---|---|
Chromosome Location | chr1:217292522-217292523 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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(count:3 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs10495041 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11576806 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11579927 | 0.88[AMR][1000 genomes] |
rs11587946 | 1.00[AFR][1000 genomes] |
rs12729753 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs12739810 | 0.87[AMR][1000 genomes] |
rs12749238 | 1.00[AFR][1000 genomes] |
rs12756259 | 1.00[AFR][1000 genomes] |
rs1502356 | 0.94[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs17695327 | 1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs35478056 | 0.88[AMR][1000 genomes] |
rs35685026 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35778506 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35963574 | 0.88[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv428610 | chr1:217143317-217307243 | Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | nsv441737 | chr1:217290125-217294328 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
3 | nsv514044 | chr1:217290161-217293537 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |