Variant report
Variant | rs6592369 |
---|---|
Chromosome Location | chr11:87207230-87207231 |
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 |
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rs_ID | r2[population] |
---|---|
rs10898702 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs10898703 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs10898713 | 0.84[ASN][1000 genomes] |
rs10898714 | 0.84[ASN][1000 genomes] |
rs10898715 | 0.84[ASN][1000 genomes] |
rs11235160 | 1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs11235163 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11235172 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11235173 | 0.84[ASN][1000 genomes] |
rs11235174 | 0.95[ASN][1000 genomes] |
rs11600506 | 0.84[ASN][1000 genomes] |
rs12362481 | 0.82[ASN][1000 genomes] |
rs2375031 | 0.84[CHB][hapmap];0.81[CHD][hapmap];0.84[JPT][hapmap] |
rs7113624 | 0.85[ASN][1000 genomes] |
rs7114049 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7114224 | 0.83[ASN][1000 genomes] |
rs7117800 | 0.83[ASN][1000 genomes] |
rs7118093 | 0.83[ASN][1000 genomes] |
rs7129725 | 0.82[ASN][1000 genomes] |
rs7129822 | 0.83[ASN][1000 genomes] |
rs73524899 | 0.92[ASN][1000 genomes] |
rs7925637 | 0.84[ASN][1000 genomes] |
rs7927877 | 0.83[ASN][1000 genomes] |
rs9645704 | 0.83[ASN][1000 genomes] |
rs9645705 | 0.83[ASN][1000 genomes] |
rs9645706 | 0.84[ASN][1000 genomes] |
rs9651757 | 0.84[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1043562 | chr11:86755535-87547185 | Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 13 gene(s) | inside rSNPs | diseases |
2 | nsv541120 | chr11:86755535-87547185 | Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 13 gene(s) | inside rSNPs | diseases |
3 | nsv555714 | chr11:87058981-87399218 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
4 | nsv1039172 | chr11:87068731-87385458 | Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | nsv832224 | chr11:87162121-87355923 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
6 | esv3347109 | chr11:87163383-87245753 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
7 | esv3357299 | chr11:87163584-87245523 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
8 | nsv1041197 | chr11:87185278-87227163 | Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:87204800-87207800 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
2 | chr11:87206200-87207800 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
3 | chr11:87206400-87209400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |