Variant report
Variant | rs851814 |
---|---|
Chromosome Location | chr7:147226358-147226359 |
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] |
---|---|
rs10250939 | 0.84[GIH][hapmap] |
rs10257834 | 0.84[GIH][hapmap] |
rs10266173 | 0.84[GIH][hapmap] |
rs10269376 | 0.84[GIH][hapmap] |
rs2074715 | 0.84[GIH][hapmap] |
rs2240376 | 0.84[GIH][hapmap] |
rs6952758 | 0.84[GIH][hapmap] |
rs6957033 | 0.84[GIH][hapmap] |
rs6962824 | 0.84[GIH][hapmap] |
rs6980002 | 0.84[GIH][hapmap] |
rs6980460 | 0.84[GIH][hapmap] |
rs851823 | 0.84[GIH][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv931005 | chr7:146730472-147381257 | Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 7 gene(s) | inside rSNPs | diseases |