Variant report
Variant | rs779986 |
---|---|
Chromosome Location | chr2:125002089-125002090 |
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] |
---|---|
rs10173293 | 0.95[ASN][1000 genomes] |
rs10197517 | 0.91[CHB][hapmap];0.95[JPT][hapmap] |
rs10496632 | 0.83[CHB][hapmap] |
rs1170618 | 0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1170632 | 1.00[CEU][hapmap];0.96[CHB][hapmap];0.95[JPT][hapmap] |
rs1170635 | 0.94[ASN][1000 genomes] |
rs12711674 | 0.91[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes] |
rs12711676 | 0.91[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes] |
rs13391053 | 0.91[CHB][hapmap];1.00[JPT][hapmap] |
rs13395031 | 0.95[ASN][1000 genomes] |
rs13403332 | 0.95[CHB][hapmap];0.95[JPT][hapmap] |
rs2901199 | 0.96[ASN][1000 genomes] |
rs34213745 | 0.94[ASN][1000 genomes] |
rs6541944 | 0.94[ASN][1000 genomes] |
rs6707012 | 0.94[ASN][1000 genomes] |
rs6719774 | 0.95[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes] |
rs7424259 | 0.91[CHB][hapmap];1.00[JPT][hapmap] |
rs7558880 | 0.91[CHB][hapmap];0.95[JPT][hapmap] |
rs779989 | 1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs779991 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap] |
rs779992 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531408 | chr2:124727329-125011247 | Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv874989 | chr2:124892592-125176030 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:125001600-125002800 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |