Variant report
Variant | rs7579655 |
---|---|
Chromosome Location | chr2:189541807-189541808 |
allele | C/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] |
---|---|
rs10804021 | 1.00[CEU][hapmap] |
rs10931368 | 0.86[EUR][1000 genomes] |
rs11676569 | 1.00[EUR][1000 genomes] |
rs11678035 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11679949 | 1.00[CEU][hapmap];1.00[CHB][hapmap] |
rs11682895 | 1.00[CHB][hapmap] |
rs11685643 | 1.00[CEU][hapmap];1.00[CHB][hapmap] |
rs11688482 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11692432 | 0.82[EUR][1000 genomes] |
rs11695177 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes] |
rs11695316 | 1.00[CEU][hapmap] |
rs12475894 | 1.00[CEU][hapmap] |
rs12476413 | 1.00[CEU][hapmap] |
rs12997039 | 1.00[CEU][hapmap] |
rs13025659 | 1.00[CEU][hapmap] |
rs13392850 | 1.00[CEU][hapmap] |
rs13393057 | 1.00[CEU][hapmap] |
rs13396968 | 1.00[CEU][hapmap] |
rs13412448 | 1.00[CEU][hapmap] |
rs13414327 | 1.00[CEU][hapmap] |
rs13418031 | 1.00[CEU][hapmap] |
rs1507551 | 1.00[CEU][hapmap] |
rs34323074 | 0.86[EUR][1000 genomes] |
rs4667231 | 1.00[CEU][hapmap] |
rs56805876 | 0.89[AFR][1000 genomes] |
rs57210291 | 0.86[EUR][1000 genomes] |
rs58512807 | 0.82[AFR][1000 genomes] |
rs60894296 | 0.86[EUR][1000 genomes] |
rs61500341 | 0.80[EUR][1000 genomes] |
rs6707212 | 1.00[CEU][hapmap] |
rs6710263 | 1.00[YRI][hapmap] |
rs6714395 | 0.85[YRI][hapmap] |
rs6756504 | 1.00[CEU][hapmap] |
rs72896869 | 0.86[EUR][1000 genomes] |
rs72896876 | 0.86[EUR][1000 genomes] |
rs72896879 | 0.86[EUR][1000 genomes] |
rs72896898 | 0.86[EUR][1000 genomes] |
rs72898830 | 0.86[EUR][1000 genomes] |
rs72898840 | 0.86[EUR][1000 genomes] |
rs72898843 | 0.86[EUR][1000 genomes] |
rs72898858 | 0.86[EUR][1000 genomes] |
rs72898866 | 0.86[EUR][1000 genomes] |
rs72898876 | 0.86[EUR][1000 genomes] |
rs72898887 | 0.86[EUR][1000 genomes] |
rs72898898 | 0.86[EUR][1000 genomes] |
rs72900830 | 0.86[EUR][1000 genomes] |
rs72900842 | 0.86[EUR][1000 genomes] |
rs72900845 | 0.86[EUR][1000 genomes] |
rs72900848 | 0.86[EUR][1000 genomes] |
rs72900849 | 0.86[EUR][1000 genomes] |
rs72900852 | 1.00[EUR][1000 genomes] |
rs72900854 | 1.00[EUR][1000 genomes] |
rs72900855 | 1.00[EUR][1000 genomes] |
rs72900857 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72900861 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72900862 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72900870 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72900874 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72900893 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72900899 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72902608 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72902642 | 1.00[ASN][1000 genomes] |
rs72902659 | 0.86[EUR][1000 genomes] |
rs72904699 | 0.86[EUR][1000 genomes] |
rs72906610 | 0.86[EUR][1000 genomes] |
rs7419798 | 1.00[CEU][hapmap] |
rs7420808 | 1.00[CEU][hapmap] |
rs7421510 | 1.00[CEU][hapmap];1.00[CHB][hapmap] |
rs7423329 | 1.00[CEU][hapmap] |
rs7423554 | 1.00[CEU][hapmap] |
rs7579593 | 1.00[CEU][hapmap];1.00[CHB][hapmap] |
rs7582643 | 1.00[CEU][hapmap] |
rs7587596 | 1.00[CEU][hapmap] |
rs7602180 | 1.00[CEU][hapmap] |
rs781261 | 1.00[CHB][hapmap] |
rs781280 | 1.00[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1003974 | chr2:189331760-189827814 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:189539400-189542400 | Enhancers | HSMM | muscle |
2 | chr2:189539600-189543400 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
3 | chr2:189540000-189542400 | Enhancers | Osteobl | bone |
4 | chr2:189540200-189542200 | Enhancers | NHDF-Ad | bronchial |
5 | chr2:189540800-189542400 | Enhancers | Muscle Satellite Cultured Cells | -- |
6 | chr2:189541200-189545000 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
7 | chr2:189541600-189543400 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |