Variant report
Variant | rs7571244 |
---|---|
Chromosome Location | chr2:125612417-125612418 |
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] |
---|---|
rs10165137 | 1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap] |
rs10168923 | 1.00[GIH][hapmap];1.00[TSI][hapmap] |
rs10172428 | 1.00[CEU][hapmap] |
rs10182183 | 1.00[CEU][hapmap] |
rs10187198 | 1.00[EUR][1000 genomes] |
rs10202474 | 1.00[CEU][hapmap];1.00[EUR][1000 genomes] |
rs10204235 | 1.00[CEU][hapmap] |
rs10210543 | 0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap] |
rs11886397 | 1.00[CEU][hapmap];0.83[YRI][hapmap];1.00[EUR][1000 genomes] |
rs11904176 | 1.00[CEU][hapmap] |
rs13403519 | 1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap] |
rs13414179 | 1.00[CEU][hapmap] |
rs17012102 | 1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap] |
rs17012116 | 0.85[GIH][hapmap];1.00[TSI][hapmap] |
rs17012123 | 1.00[GIH][hapmap];1.00[TSI][hapmap] |
rs1840209 | 0.85[GIH][hapmap];1.00[TSI][hapmap] |
rs1840210 | 1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap] |
rs62171358 | 1.00[EUR][1000 genomes] |
rs62173261 | 1.00[EUR][1000 genomes] |
rs73955848 | 1.00[EUR][1000 genomes] |
rs73955852 | 1.00[EUR][1000 genomes] |
rs7559266 | 1.00[CEU][hapmap] |
rs7567297 | 1.00[EUR][1000 genomes] |
rs7604892 | 1.00[CEU][hapmap];1.00[EUR][1000 genomes] |
rs7605407 | 1.00[CEU][hapmap];1.00[EUR][1000 genomes] |
rs7606120 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv834360 | chr2:125492685-125683200 | Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | nsv834361 | chr2:125601081-125810992 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
No data |