Variant report
Variant | rs11014564 |
---|---|
Chromosome Location | chr10:25732995-25732996 |
allele | G/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:
1
No data |
No data |
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No data |
rs_ID | r2[population] |
---|---|
rs10399962 | 0.88[CEU][hapmap];0.94[EUR][1000 genomes] |
rs10741087 | 0.94[EUR][1000 genomes] |
rs10764543 | 0.88[CEU][hapmap] |
rs10828793 | 0.88[CEU][hapmap] |
rs10828807 | 0.88[CEU][hapmap] |
rs11014530 | 0.88[CEU][hapmap] |
rs11014550 | 0.82[CEU][hapmap] |
rs11014553 | 0.88[CEU][hapmap] |
rs11014554 | 0.88[CEU][hapmap] |
rs11014558 | 0.83[CEU][hapmap];0.84[GIH][hapmap];0.93[EUR][1000 genomes] |
rs11014559 | 0.88[CEU][hapmap];0.94[EUR][1000 genomes] |
rs11014560 | 0.94[EUR][1000 genomes] |
rs11014561 | 0.81[EUR][1000 genomes] |
rs12259043 | 0.88[CEU][hapmap] |
rs12259696 | 0.88[CEU][hapmap] |
rs12356315 | 0.94[CEU][hapmap];0.86[CHB][hapmap];0.82[CHD][hapmap] |
rs12358447 | 0.94[CEU][hapmap] |
rs12764415 | 1.00[CEU][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap] |
rs12765005 | 1.00[CEU][hapmap] |
rs12770990 | 1.00[CEU][hapmap] |
rs12773262 | 0.93[CEU][hapmap] |
rs16925850 | 0.88[CEU][hapmap] |
rs16925877 | 1.00[CEU][hapmap] |
rs4431923 | 0.88[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3349863 | chr10:25614571-25946379 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |