Variant report
Variant | rs957737 |
---|---|
Chromosome Location | chr8:111820603-111820604 |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs11988217 | 1.00[EUR][1000 genomes] |
rs11992030 | 1.00[EUR][1000 genomes] |
rs11992740 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11994333 | 1.00[EUR][1000 genomes] |
rs16881058 | 1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4270933 | 1.00[EUR][1000 genomes] |
rs4276660 | 1.00[EUR][1000 genomes] |
rs57140595 | 0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58124990 | 1.00[EUR][1000 genomes] |
rs60351304 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6992503 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6997576 | 1.00[EUR][1000 genomes] |
rs73315859 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73315898 | 1.00[EUR][1000 genomes] |
rs73316607 | 1.00[EUR][1000 genomes] |
rs73317247 | 1.00[EUR][1000 genomes] |
rs73317294 | 1.00[EUR][1000 genomes] |
rs73317962 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73317974 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73317977 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73319771 | 1.00[EUR][1000 genomes] |
rs73324493 | 1.00[EUR][1000 genomes] |
rs73332950 | 1.00[EUR][1000 genomes] |
rs73332956 | 1.00[EUR][1000 genomes] |
rs73332960 | 1.00[EUR][1000 genomes] |
rs7463050 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7837586 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1027659 | chr8:111585843-111875753 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv831423 | chr8:111672801-111869818 | Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv891293 | chr8:111704563-111822043 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | n/a |
4 | nsv1031245 | chr8:111716585-111875753 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | nsv891294 | chr8:111754075-112163801 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
6 | nsv1032766 | chr8:111779352-111995438 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
7 | nsv1030494 | chr8:111779352-112421812 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
8 | esv2754849 | chr8:111817591-112088992 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:111788600-111826200 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
2 | chr8:111818800-111821000 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
3 | chr8:111820200-111821000 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
4 | chr8:111820600-111821000 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |