Variant report
Variant | rs7738754 |
---|---|
Chromosome Location | chr6:127206932-127206933 |
allele | A/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] |
---|---|
rs10484756 | 1.00[EUR][1000 genomes] |
rs17053217 | 0.88[AMR][1000 genomes] |
rs17054080 | 0.97[EUR][1000 genomes] |
rs17054134 | 1.00[EUR][1000 genomes] |
rs17054160 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17054190 | 0.88[AMR][1000 genomes] |
rs17054191 | 0.88[AMR][1000 genomes] |
rs17054195 | 0.82[AMR][1000 genomes] |
rs17054204 | 0.82[AMR][1000 genomes] |
rs1930953 | 0.82[AMR][1000 genomes] |
rs1970592 | 1.00[EUR][1000 genomes] |
rs1999559 | 0.88[AMR][1000 genomes] |
rs2153990 | 1.00[EUR][1000 genomes] |
rs56721799 | 0.80[AMR][1000 genomes] |
rs62439182 | 0.80[AMR][1000 genomes] |
rs62439186 | 0.80[AMR][1000 genomes] |
rs6569472 | 0.82[AMR][1000 genomes] |
rs6917816 | 0.88[AMR][1000 genomes] |
rs6918236 | 0.88[AMR][1000 genomes] |
rs6918438 | 0.88[AMR][1000 genomes] |
rs6930028 | 0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6930721 | 1.00[EUR][1000 genomes] |
rs6934463 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6941470 | 0.88[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1026498 | chr6:126812609-127397240 | Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
2 | nsv1024206 | chr6:126873187-127475713 | Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
3 | nsv538438 | chr6:126873187-127475713 | Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
4 | nsv1020322 | chr6:127087551-127331285 | Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | Chromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:127200800-127207200 | Weak transcription | HUVEC | blood vessel |
2 | chr6:127206400-127208000 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |