Variant report
Variant | rs6907179 |
---|---|
Chromosome Location | chr6:71631823-71631824 |
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] |
---|---|
rs10945278 | 0.91[EUR][1000 genomes] |
rs11757574 | 0.91[EUR][1000 genomes] |
rs11759339 | 0.96[CEU][hapmap];1.00[CHB][hapmap] |
rs12524190 | 0.91[EUR][1000 genomes] |
rs12529422 | 0.91[EUR][1000 genomes] |
rs16869607 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap] |
rs2347632 | 0.91[EUR][1000 genomes] |
rs2347633 | 0.91[EUR][1000 genomes] |
rs4479893 | 0.90[EUR][1000 genomes] |
rs4506005 | 0.91[EUR][1000 genomes] |
rs55870610 | 0.92[EUR][1000 genomes] |
rs56291137 | 0.89[EUR][1000 genomes] |
rs6900853 | 0.83[CEU][hapmap] |
rs6911809 | 1.00[CHB][hapmap] |
rs6927786 | 0.89[EUR][1000 genomes] |
rs72920735 | 0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs7451863 | 0.91[EUR][1000 genomes] |
rs7746949 | 0.91[EUR][1000 genomes] |
rs7774025 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs9283838 | 0.88[EUR][1000 genomes] |
rs9294883 | 0.91[EUR][1000 genomes] |
rs9354961 | 1.00[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv932111 | chr6:70736835-71633094 | Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 31 gene(s) | inside rSNPs | diseases |
2 | nsv886148 | chr6:71623253-71694742 | Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |