Variant report
Variant | rs10756495 |
---|---|
Chromosome Location | chr9:13762174-13762175 |
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] |
---|---|
rs10738347 | 0.91[EUR][1000 genomes] |
rs10738348 | 0.84[EUR][1000 genomes] |
rs10756502 | 0.89[EUR][1000 genomes] |
rs10756506 | 0.84[EUR][1000 genomes] |
rs10810016 | 0.83[AMR][1000 genomes] |
rs10810024 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs10810028 | 0.87[EUR][1000 genomes] |
rs10961219 | 0.81[AMR][1000 genomes] |
rs10961227 | 0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10961228 | 0.94[AFR][1000 genomes];0.94[EUR][1000 genomes] |
rs10961232 | 0.91[EUR][1000 genomes] |
rs10961234 | 0.89[EUR][1000 genomes] |
rs10961243 | 0.83[EUR][1000 genomes] |
rs11789856 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12378052 | 0.89[EUR][1000 genomes] |
rs12555747 | 0.88[AMR][1000 genomes] |
rs12555754 | 0.88[AMR][1000 genomes] |
rs17216585 | 0.87[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs17217956 | 0.83[EUR][1000 genomes] |
rs17217996 | 0.83[EUR][1000 genomes] |
rs55871307 | 0.91[EUR][1000 genomes] |
rs62533246 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs62534674 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs62534675 | 0.87[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs7024746 | 0.85[EUR][1000 genomes] |
rs72711965 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs745034 | 0.85[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv892590 | chr9:13689066-13777299 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | nsv1022001 | chr9:13717736-13983738 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:13758200-13787200 | Weak transcription | Aorta | Aorta |
2 | chr9:13760000-13764600 | Weak transcription | Fetal Muscle Leg | muscle |