Variant report
Variant | rs12255610 |
---|---|
Chromosome Location | chr10:56028635-56028636 |
allele | C/T |
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] |
---|---|
rs10218915 | 1.00[CEU][hapmap];0.89[EUR][1000 genomes] |
rs10400005 | 1.00[JPT][hapmap] |
rs10825275 | 1.00[JPT][hapmap] |
rs10825277 | 1.00[JPT][hapmap] |
rs10825278 | 1.00[JPT][hapmap] |
rs10825285 | 1.00[JPT][hapmap] |
rs11004139 | 1.00[JPT][hapmap] |
rs11004148 | 1.00[CEU][hapmap] |
rs11004151 | 1.00[CEU][hapmap];0.89[EUR][1000 genomes] |
rs11004166 | 1.00[CEU][hapmap] |
rs11004175 | 1.00[CEU][hapmap] |
rs11004179 | 1.00[JPT][hapmap] |
rs11004181 | 1.00[JPT][hapmap] |
rs11004183 | 0.88[LWK][hapmap];0.94[YRI][hapmap] |
rs11004185 | 1.00[JPT][hapmap];0.84[LWK][hapmap];0.94[YRI][hapmap] |
rs12240793 | 0.89[EUR][1000 genomes] |
rs12240800 | 0.89[EUR][1000 genomes] |
rs12242872 | 1.00[CEU][hapmap] |
rs12245058 | 1.00[CEU][hapmap] |
rs12245249 | 1.00[CEU][hapmap] |
rs12248220 | 1.00[CEU][hapmap];0.89[EUR][1000 genomes] |
rs12250056 | 0.89[EUR][1000 genomes] |
rs12250885 | 1.00[JPT][hapmap];0.83[YRI][hapmap];1.00[ASN][1000 genomes] |
rs12252710 | 0.89[EUR][1000 genomes] |
rs12252904 | 0.89[EUR][1000 genomes] |
rs12258533 | 1.00[JPT][hapmap] |
rs12260244 | 1.00[CEU][hapmap] |
rs12260476 | 1.00[CEU][hapmap] |
rs12261438 | 1.00[CEU][hapmap] |
rs12261807 | 0.89[EUR][1000 genomes] |
rs12268918 | 1.00[CEU][hapmap];1.00[JPT][hapmap] |
rs7069137 | 1.00[CEU][hapmap] |
rs7077036 | 1.00[EUR][1000 genomes] |
rs7078086 | 1.00[JPT][hapmap];0.89[YRI][hapmap] |
rs7086633 | 1.00[CEU][hapmap] |
rs7090842 | 1.00[CEU][hapmap] |
rs713274 | 1.00[CEU][hapmap] |
rs7893562 | 1.00[JPT][hapmap] |
rs7893808 | 1.00[JPT][hapmap] |
rs7896210 | 1.00[CEU][hapmap] |
rs7899424 | 0.89[EUR][1000 genomes] |
rs7899428 | 0.89[EUR][1000 genomes] |
rs7902567 | 0.89[EUR][1000 genomes] |
rs7902932 | 0.89[EUR][1000 genomes] |
rs7906179 | 0.89[EUR][1000 genomes] |
rs7910314 | 1.00[CEU][hapmap] |
rs7911444 | 1.00[CEU][hapmap] |
rs7913738 | 0.89[EUR][1000 genomes] |
rs7915325 | 0.89[EUR][1000 genomes] |
rs7915552 | 1.00[CEU][hapmap];0.89[EUR][1000 genomes] |
rs7918079 | 0.89[EUR][1000 genomes] |
rs7919046 | 1.00[CEU][hapmap];0.89[EUR][1000 genomes] |
rs7923915 | 1.00[JPT][hapmap] |
rs9804255 | 1.00[JPT][hapmap];0.88[YRI][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv870252 | chr10:55823123-56029435 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
2 | nsv948730 | chr10:55845301-56093271 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | esv2829924 | chr10:55906112-56038831 | Weak transcription Enhancers Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv1054364 | chr10:55925471-56196447 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | nsv540633 | chr10:55925471-56196447 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
6 | esv20105 | chr10:55939729-56047721 | ZNF genes & repeats Enhancers Weak transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | nsv1053832 | chr10:56022197-56061600 | Enhancers Weak transcription | n/a | n/a | inside rSNPs | diseases |
8 | esv2753511 | chr10:56022197-56153636 | Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |