Variant report
Variant | rs9384546 |
---|---|
Chromosome Location | chr6:150826652-150826653 |
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] |
---|---|
rs1492574 | 0.80[ASN][1000 genomes] |
rs4304173 | 0.94[ASN][1000 genomes] |
rs4478418 | 0.89[ASN][1000 genomes] |
rs6903974 | 0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs6908890 | 0.87[ASN][1000 genomes] |
rs6913362 | 0.80[ASN][1000 genomes] |
rs7745789 | 0.88[ASN][1000 genomes] |
rs7764084 | 0.83[ASN][1000 genomes] |
rs9322262 | 0.81[ASN][1000 genomes] |
rs9371454 | 0.82[ASN][1000 genomes] |
rs9371461 | 0.81[ASN][1000 genomes] |
rs9372055 | 0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs9372056 | 0.82[ASN][1000 genomes] |
rs9383828 | 0.82[ASN][1000 genomes] |
rs9384547 | 0.84[ASN][1000 genomes] |
rs9384551 | 0.91[ASN][1000 genomes] |
rs9384557 | 0.85[ASN][1000 genomes] |
rs9397324 | 0.82[ASN][1000 genomes] |
rs9397330 | 0.91[ASN][1000 genomes] |
rs9398010 | 0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9480466 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs9480468 | 0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1020067 | chr6:150730783-150870708 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv886772 | chr6:150743364-151024280 | Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:150825000-150830800 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |