Variant report
Variant | rs11023525 |
---|---|
Chromosome Location | chr11:15333882-15333883 |
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] |
---|---|
rs11023518 | 0.96[EUR][1000 genomes] |
rs11023523 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11023537 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs11023542 | 0.94[EUR][1000 genomes] |
rs11023543 | 0.94[EUR][1000 genomes] |
rs11023547 | 0.94[EUR][1000 genomes] |
rs11023555 | 0.83[EUR][1000 genomes] |
rs11023568 | 0.86[EUR][1000 genomes] |
rs12363177 | 0.94[EUR][1000 genomes] |
rs12577240 | 0.94[EUR][1000 genomes] |
rs12800836 | 0.94[EUR][1000 genomes] |
rs35824480 | 0.93[EUR][1000 genomes] |
rs4604863 | 0.94[EUR][1000 genomes] |
rs67068849 | 0.94[EUR][1000 genomes] |
rs67732927 | 0.94[EUR][1000 genomes] |
rs67828350 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72861982 | 0.94[EUR][1000 genomes] |
rs72861992 | 0.90[EUR][1000 genomes] |
rs9645645 | 0.94[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2830370 | chr11:15142247-15444094 | Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
2 | nsv832072 | chr11:15226843-15392190 | Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:15330000-15338800 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |