Variant report
Variant | rs6845307 |
---|---|
Chromosome Location | chr4:26535661-26535662 |
allele | C/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] |
---|---|
rs12651350 | 1.00[EUR][1000 genomes] |
rs36224744 | 1.00[EUR][1000 genomes] |
rs36224745 | 1.00[EUR][1000 genomes] |
rs4349588 | 1.00[TSI][hapmap] |
rs4692548 | 1.00[EUR][1000 genomes] |
rs56656455 | 1.00[EUR][1000 genomes] |
rs56834351 | 1.00[EUR][1000 genomes] |
rs57269196 | 1.00[EUR][1000 genomes] |
rs58297498 | 1.00[EUR][1000 genomes] |
rs58551878 | 1.00[EUR][1000 genomes] |
rs58990586 | 1.00[EUR][1000 genomes] |
rs59082948 | 1.00[EUR][1000 genomes] |
rs59902050 | 1.00[EUR][1000 genomes] |
rs60016776 | 1.00[EUR][1000 genomes] |
rs60212470 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60373412 | 1.00[EUR][1000 genomes] |
rs60930192 | 1.00[EUR][1000 genomes] |
rs61179790 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61239973 | 1.00[EUR][1000 genomes] |
rs61299741 | 1.00[EUR][1000 genomes] |
rs61557900 | 1.00[EUR][1000 genomes] |
rs61681337 | 1.00[EUR][1000 genomes] |
rs6825731 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6838102 | 1.00[EUR][1000 genomes] |
rs6839766 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7659656 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7680701 | 1.00[AMR][1000 genomes] |
rs7683070 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7689334 | 1.00[EUR][1000 genomes] |
rs9291485 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2762417 | chr4:26491768-26576800 | Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:26532200-26536600 | Weak transcription | HSMMtube | muscle |
2 | chr4:26535600-26535800 | Enhancers | iPS-20b Cell Line | embryonic stem cell |