Variant report
Variant | rs6036718 |
---|---|
Chromosome Location | chr20:24265651-24265652 |
allele | C/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] |
---|---|
rs6036707 | 0.81[EUR][1000 genomes] |
rs6036709 | 0.85[EUR][1000 genomes] |
rs6036731 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6049549 | 0.81[EUR][1000 genomes] |
rs6049550 | 0.81[EUR][1000 genomes] |
rs6049553 | 0.85[EUR][1000 genomes] |
rs6049557 | 0.96[EUR][1000 genomes] |
rs6049561 | 0.96[EUR][1000 genomes] |
rs6049562 | 0.96[EUR][1000 genomes] |
rs6049564 | 0.85[EUR][1000 genomes] |
rs6049566 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6049567 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6049568 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6049572 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6049573 | 0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6076217 | 1.00[ASN][1000 genomes] |
rs6083473 | 1.00[ASN][1000 genomes] |
rs6083480 | 1.00[ASN][1000 genomes] |
rs6083481 | 0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6083484 | 1.00[ASN][1000 genomes] |
rs6083486 | 1.00[ASN][1000 genomes] |
rs6083487 | 1.00[ASN][1000 genomes] |
rs6083488 | 1.00[ASN][1000 genomes] |
rs6106812 | 0.85[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv9793 | chr20:23939613-24734850 | Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
2 | esv3328348 | chr20:24095746-24285830 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
3 | nsv833945 | chr20:24163437-24349462 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
4 | nsv1058146 | chr20:24210196-24531087 | Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr20:24264000-24270400 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
2 | chr20:24265200-24267400 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |