Variant report
Variant | rs12056447 |
---|---|
Chromosome Location | chr8:64062258-64062259 |
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] |
---|---|
rs10957275 | 0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10957276 | 0.86[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12056437 | 0.90[ASN][1000 genomes] |
rs12056441 | 0.86[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs12542182 | 0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs12542741 | 0.93[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs12547669 | 0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs12549833 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs12550222 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs12550793 | 0.96[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs12677153 | 0.81[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs12678231 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs1975246 | 0.85[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs2241753 | 0.84[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs34803356 | 0.93[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs3857972 | 0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs3929126 | 0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs4601308 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs4739053 | 0.96[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs6983011 | 0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs7000495 | 0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs7000788 | 0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs7000927 | 0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs7001014 | 0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs73254967 | 0.92[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs73254968 | 0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs73684686 | 0.85[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs73684689 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs9643383 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs9643384 | 0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs9643556 | 0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9643557 | 0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs9643558 | 0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1033527 | chr8:63673915-64073735 | Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
2 | nsv465701 | chr8:63951237-64080486 | Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
3 | nsv611448 | chr8:63951237-64080486 | Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
4 | nsv890965 | chr8:64006201-64104092 | Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
5 | esv9765 | chr8:64059438-64065076 | Flanking Active TSS Enhancers Active TSS Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:64061800-64063200 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |