Variant report
Variant | rs61467163 |
---|---|
Chromosome Location | chr8:110369276-110369277 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
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(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs10093885 | 1.00[ASN][1000 genomes] |
rs10100944 | 1.00[ASN][1000 genomes] |
rs10108704 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11778756 | 1.00[ASN][1000 genomes] |
rs11784792 | 1.00[ASN][1000 genomes] |
rs11785973 | 1.00[ASN][1000 genomes] |
rs13438836 | 1.00[ASN][1000 genomes] |
rs1563581 | 1.00[ASN][1000 genomes] |
rs17368044 | 1.00[ASN][1000 genomes] |
rs17445342 | 1.00[ASN][1000 genomes] |
rs17446406 | 1.00[ASN][1000 genomes] |
rs28463252 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28491535 | 0.81[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs55800074 | 1.00[ASN][1000 genomes] |
rs59237049 | 1.00[ASN][1000 genomes] |
rs60189528 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6469255 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6982826 | 0.83[AMR][1000 genomes] |
rs6999170 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs7008687 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs72682697 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72684719 | 1.00[ASN][1000 genomes] |
rs72684799 | 1.00[ASN][1000 genomes] |
rs72687010 | 1.00[ASN][1000 genomes] |
rs72687015 | 1.00[ASN][1000 genomes] |
rs7816624 | 1.00[ASN][1000 genomes] |
rs7817639 | 1.00[ASN][1000 genomes] |
rs7818929 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7820734 | 1.00[ASN][1000 genomes] |
rs7835131 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs7836433 | 0.81[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9656791 | 1.00[ASN][1000 genomes] |
rs9656881 | 0.87[AMR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv891273 | chr8:110219735-110475874 | Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
2 | nsv891279 | chr8:110268104-110450092 | Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
3 | nsv891280 | chr8:110346363-110465481 | Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:110364800-110374800 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
2 | chr8:110367400-110372600 | Weak transcription | K562 | blood |