Variant report
Variant | rs28583803 |
---|---|
Chromosome Location | chr8:110819126-110819127 |
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] |
---|---|
rs10086058 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10091536 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10091583 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs10097751 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10101288 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10102735 | 1.00[ASN][1000 genomes] |
rs16879889 | 1.00[EUR][1000 genomes] |
rs16879906 | 1.00[EUR][1000 genomes] |
rs28423669 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28571606 | 1.00[EUR][1000 genomes] |
rs28593097 | 1.00[EUR][1000 genomes] |
rs28610171 | 1.00[EUR][1000 genomes] |
rs28623195 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4313130 | 1.00[EUR][1000 genomes] |
rs57167766 | 1.00[EUR][1000 genomes] |
rs57285880 | 1.00[EUR][1000 genomes] |
rs57962861 | 1.00[EUR][1000 genomes] |
rs58404081 | 1.00[EUR][1000 genomes] |
rs58910462 | 1.00[EUR][1000 genomes] |
rs59161508 | 1.00[EUR][1000 genomes] |
rs59981669 | 1.00[EUR][1000 genomes] |
rs60387056 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs60841208 | 1.00[EUR][1000 genomes] |
rs73319188 | 1.00[EUR][1000 genomes] |
rs73319190 | 1.00[EUR][1000 genomes] |
rs7817773 | 1.00[EUR][1000 genomes] |
rs7825511 | 1.00[EUR][1000 genomes] |
rs7825600 | 1.00[EUR][1000 genomes] |
rs7825601 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv611880 | chr8:110762913-110821596 | Enhancers Weak transcription ZNF genes & repeats | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:110819000-110820200 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
2 | chr8:110819000-110821400 | Enhancers | Fetal Heart | heart |