Variant report
Variant | rs2092413 |
---|---|
Chromosome Location | chr6:54297501-54297502 |
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] |
---|---|
rs10948827 | 0.88[ASN][1000 genomes] |
rs12526335 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12529259 | 0.84[ASN][1000 genomes] |
rs1303838 | 0.84[ASN][1000 genomes] |
rs13201322 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1648211 | 0.83[ASN][1000 genomes] |
rs17828849 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs1895835 | 0.84[ASN][1000 genomes] |
rs3909649 | 0.88[ASN][1000 genomes] |
rs4715462 | 0.88[ASN][1000 genomes] |
rs567013 | 0.87[ASN][1000 genomes] |
rs605743 | 0.83[ASN][1000 genomes] |
rs683560 | 0.83[ASN][1000 genomes] |
rs7450725 | 0.84[ASN][1000 genomes] |
rs9464088 | 0.84[ASN][1000 genomes] |
rs9464089 | 0.84[ASN][1000 genomes] |
rs9464091 | 0.88[ASN][1000 genomes] |
rs9464092 | 0.88[ASN][1000 genomes] |
rs9464093 | 0.88[ASN][1000 genomes] |
rs9474878 | 0.85[ASN][1000 genomes] |
rs9474879 | 0.85[ASN][1000 genomes] |
rs9474882 | 0.81[ASN][1000 genomes] |
rs9474888 | 0.86[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1067663 | chr6:53796341-54449718 | Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
2 | nsv529158 | chr6:53796341-54449718 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
3 | nsv528901 | chr6:54290333-54337130 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv427757 | chr6:54296552-54507210 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:54296400-54297600 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |