Variant report
Variant | rs11211945 |
---|---|
Chromosome Location | chr11:106722896-106722897 |
allele | A/C |
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] |
---|---|
rs11211920 | 0.83[ASN][1000 genomes] |
rs11211938 | 0.81[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs11211939 | 0.82[ASN][1000 genomes] |
rs11524439 | 0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12363827 | 0.81[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs1487890 | 0.83[ASN][1000 genomes] |
rs17651489 | 0.82[ASN][1000 genomes] |
rs1944195 | 0.82[ASN][1000 genomes] |
rs35636240 | 0.97[ASN][1000 genomes] |
rs67110749 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7109075 | 0.95[ASN][1000 genomes] |
rs7113801 | 0.81[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv898362 | chr11:106715879-106809457 | ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
2 | nsv1036990 | chr11:106718613-106774766 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv541162 | chr11:106718613-106774766 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:106719200-106730400 | Weak transcription | Fetal Lung | lung |