Variant report
Variant | rs9589584 |
---|---|
Chromosome Location | chr13:93232301-93232302 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr13:93187246..93189629-chr13:93231804..93233615,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs16947779 | 1.00[ASW][hapmap];1.00[CEU][hapmap];0.89[LWK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap] |
rs28723564 | 1.00[EUR][1000 genomes] |
rs7330553 | 1.00[CEU][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap] |
rs7983573 | 1.00[CEU][hapmap] |
rs8000850 | 1.00[CEU][hapmap] |
rs9301818 | 1.00[CEU][hapmap];1.00[EUR][1000 genomes] |
rs9301820 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9584033 | 1.00[ASW][hapmap];1.00[CEU][hapmap];0.89[LWK][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];1.00[EUR][1000 genomes] |
rs9584035 | 1.00[CEU][hapmap];1.00[TSI][hapmap] |
rs9584036 | 1.00[ASW][hapmap];0.89[LWK][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap] |
rs9584037 | 1.00[ASW][hapmap];1.00[CEU][hapmap];0.89[LWK][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap] |
rs9584038 | 1.00[CEU][hapmap] |
rs9589568 | 1.00[CEU][hapmap];1.00[EUR][1000 genomes] |
rs9589569 | 1.00[EUR][1000 genomes] |
rs9589571 | 1.00[CEU][hapmap];1.00[TSI][hapmap] |
rs9589578 | 1.00[CEU][hapmap];1.00[YRI][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv456070 | chr13:93208593-93298523 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
2 | nsv562730 | chr13:93208593-93298523 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | esv1808762 | chr13:93232301-93241744 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
4 | esv1842146 | chr13:93232301-93241744 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:93226200-93235600 | Weak transcription | Right Atrium | heart |