Variant report
Variant | rs12724895 |
---|---|
Chromosome Location | chr1:159291045-159291046 |
allele | A/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)
No data |
No data |
(count:2 , 50 per page) page:
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No data |
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Variant related genes | Relation type |
---|---|
ENSG00000196266 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10908709 | 0.81[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
rs10908710 | 0.81[AFR][1000 genomes] |
rs10908720 | 0.82[JPT][hapmap] |
rs11265166 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11265204 | 0.87[CHD][hapmap] |
rs12145079 | 0.82[YRI][hapmap] |
rs2247584 | 1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.80[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs2251746 | 0.81[MKK][hapmap];1.00[YRI][hapmap] |
rs2427836 | 0.89[ASW][hapmap];0.90[MEX][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs2494251 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs2494262 | 0.89[MKK][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes] |
rs2494264 | 0.89[ASW][hapmap];0.82[CEU][hapmap];0.95[MEX][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs2511213 | 0.85[AFR][1000 genomes] |
rs2511214 | 1.00[YRI][hapmap];0.85[AFR][1000 genomes] |
rs2511215 | 0.82[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv872487 | chr1:159196765-159342439 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv872488 | chr1:159218266-159336948 | Flanking Active TSS Enhancers Weak transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |