Variant report
Variant | rs11766474 |
---|---|
Chromosome Location | chr7:14389557-14389558 |
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] |
---|---|
rs11977804 | 0.90[JPT][hapmap] |
rs11983089 | 0.91[JPT][hapmap] |
rs1319592 | 0.90[JPT][hapmap];0.84[AMR][1000 genomes] |
rs1319593 | 0.90[JPT][hapmap];0.81[AMR][1000 genomes] |
rs1469618 | 0.85[JPT][hapmap] |
rs17168087 | 0.80[CHB][hapmap];0.81[ASN][1000 genomes] |
rs17168097 | 0.91[JPT][hapmap];0.92[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs17168106 | 0.90[JPT][hapmap] |
rs17168109 | 0.90[JPT][hapmap] |
rs2217572 | 0.81[CEU][hapmap];0.95[JPT][hapmap] |
rs2357898 | 0.82[ASN][1000 genomes] |
rs4721330 | 0.95[JPT][hapmap] |
rs4721331 | 0.91[JPT][hapmap] |
rs59831821 | 0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6946703 | 0.91[JPT][hapmap] |
rs6947526 | 0.90[JPT][hapmap] |
rs6963946 | 0.90[JPT][hapmap] |
rs6971911 | 0.96[CEU][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949033 | chr7:14086106-14860323 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | esv1793644 | chr7:14385632-14391369 | Enhancers Weak transcription | n/a | n/a | inside rSNPs | diseases |
3 | nsv606281 | chr7:14388381-14443963 | Weak transcription Flanking Active TSS Enhancers Active TSS | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:14383200-14390800 | Weak transcription | Fetal Heart | heart |