Variant report
Variant | rs10739186 |
---|---|
Chromosome Location | chr9:9249969-9249970 |
allele | A/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] |
---|---|
rs10816074 | 0.82[JPT][hapmap] |
rs4132505 | 0.95[CHB][hapmap];0.95[JPT][hapmap];0.88[YRI][hapmap] |
rs4237174 | 0.84[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap] |
rs4272446 | 0.81[JPT][hapmap] |
rs4297075 | 0.82[JPT][hapmap] |
rs4344133 | 0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes] |
rs4361814 | 0.81[JPT][hapmap] |
rs4457389 | 0.81[JPT][hapmap] |
rs4560852 | 0.82[JPT][hapmap] |
rs4568657 | 0.81[JPT][hapmap] |
rs4620334 | 0.95[CHB][hapmap];0.95[JPT][hapmap] |
rs4742576 | 0.91[CHB][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap] |
rs4742579 | 0.89[YRI][hapmap] |
rs5001110 | 0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap] |
rs6477375 | 0.81[CHB][hapmap] |
rs6477376 | 0.81[AFR][1000 genomes];0.84[ASN][1000 genomes] |
rs6477377 | 1.00[YRI][hapmap] |
rs7018892 | 0.82[CHB][hapmap];0.89[YRI][hapmap] |
rs7032620 | 0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
rs7041871 | 0.83[CHB][hapmap];0.82[JPT][hapmap] |
rs7043023 | 0.89[YRI][hapmap] |
rs7859634 | 0.86[JPT][hapmap] |
rs7863177 | 0.86[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv498066 | chr9:8961722-9486652 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv892249 | chr9:9026854-9377679 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
3 | nsv831505 | chr9:9072216-9277320 | ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
4 | nsv892252 | chr9:9164473-9476425 | Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
5 | nsv1027042 | chr9:9208635-9300048 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | inside rSNPs | diseases |
6 | nsv1021440 | chr9:9231961-9329870 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS | n/a | n/a | inside rSNPs | n/a |
7 | nsv892253 | chr9:9249912-9287321 | Enhancers | n/a | n/a | inside rSNPs | n/a |
No data |