Variant report
Variant | rs1819421 |
---|---|
Chromosome Location | chr13:92561714-92561715 |
allele | G/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] |
---|---|
rs1330472 | 0.81[CHD][hapmap] |
rs1411517 | 0.84[CHD][hapmap] |
rs1571596 | 0.84[CHD][hapmap];0.83[MEX][hapmap] |
rs1854734 | 0.83[MEX][hapmap] |
rs1854735 | 0.98[ASN][1000 genomes] |
rs2352192 | 0.90[CHB][hapmap];0.84[CHD][hapmap] |
rs2352193 | 0.84[ASN][1000 genomes] |
rs2352195 | 0.85[CHB][hapmap];0.87[CHD][hapmap];0.80[JPT][hapmap];0.83[MEX][hapmap] |
rs2352197 | 0.81[ASN][1000 genomes] |
rs2352199 | 0.83[MEX][hapmap] |
rs4773655 | 0.84[CHD][hapmap];0.83[MEX][hapmap];0.81[ASN][1000 genomes] |
rs4773657 | 0.87[CHD][hapmap] |
rs7318425 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap] |
rs7321674 | 0.84[CHD][hapmap];0.83[MEX][hapmap] |
rs7332162 | 0.80[JPT][hapmap] |
rs7986596 | 0.84[CHD][hapmap] |
rs7989697 | 0.84[CHD][hapmap] |
rs9301758 | 0.95[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap] |
rs9301763 | 0.80[CHB][hapmap];0.87[CHD][hapmap];0.83[MEX][hapmap] |
rs9515990 | 0.95[CHB][hapmap];0.81[CHD][hapmap];0.92[MEX][hapmap] |
rs9523451 | 1.00[CHB][hapmap];0.94[CHD][hapmap];0.90[JPT][hapmap] |
rs9523453 | 0.81[ASN][1000 genomes] |
rs9523455 | 0.84[CHD][hapmap];0.83[MEX][hapmap] |
rs9523458 | 0.81[CHD][hapmap] |
rs9556129 | 1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes] |
rs9556131 | 0.85[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3378326 | chr13:92445514-92816367 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv900883 | chr13:92481236-92602622 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
3 | nsv976142 | chr13:92492782-92567759 | Weak transcription Enhancers Flanking Active TSS Active TSS | lncRNA | n/a | inside rSNPs | diseases |
4 | nsv900884 | chr13:92548841-92595572 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS | n/a | n/a | inside rSNPs | n/a |
5 | nsv916705 | chr13:92549110-92575114 | Enhancers Weak transcription Active TSS Flanking Active TSS | n/a | n/a | inside rSNPs | n/a |
6 | nsv983613 | chr13:92550026-92567759 | Active TSS Enhancers Weak transcription Flanking Active TSS | n/a | n/a | inside rSNPs | n/a |
7 | nsv900885 | chr13:92561714-92621620 | Weak transcription Enhancers ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |