Variant report
Variant | rs1203069 |
---|---|
Chromosome Location | chr6:120908753-120908754 |
allele | A/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] |
---|---|
rs1203066 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs1203071 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs1203072 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs1203078 | 0.92[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs1203080 | 0.80[AFR][1000 genomes] |
rs1203089 | 0.88[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs1203091 | 0.88[AFR][1000 genomes] |
rs1203092 | 0.88[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs2788665 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs2788666 | 0.88[AFR][1000 genomes] |
rs28497554 | 1.00[ASN][1000 genomes] |
rs62426588 | 0.89[ASN][1000 genomes] |
rs6569151 | 0.85[ASN][1000 genomes] |
rs9372612 | 0.89[ASN][1000 genomes] |
rs9372613 | 0.89[ASN][1000 genomes] |
rs9372622 | 1.00[ASN][1000 genomes] |
rs9385162 | 0.89[ASN][1000 genomes] |
rs9385168 | 1.00[ASN][1000 genomes] |
rs9387838 | 0.89[ASN][1000 genomes] |
rs9387854 | 1.00[ASN][1000 genomes] |
rs9387855 | 0.95[ASN][1000 genomes] |
rs9387856 | 1.00[ASN][1000 genomes] |
rs9398587 | 1.00[ASN][1000 genomes] |
rs9398588 | 1.00[ASN][1000 genomes] |
rs9401285 | 0.89[ASN][1000 genomes] |
rs9401291 | 0.89[ASN][1000 genomes] |
rs9401306 | 0.95[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2753290 | chr6:120309301-120979301 | Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS | TF binding regionChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
2 | esv2752474 | chr6:120309301-120982301 | Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS | TF binding regionChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv428495 | chr6:120861159-120954224 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
4 | esv3396982 | chr6:120900302-120916167 | Enhancers Weak transcription | n/a | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:120905600-120909800 | Enhancers | Brain Germinal Matrix | brain |