Variant report
Variant | rs2808692 |
---|---|
Chromosome Location | chr9:100490372-100490373 |
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] |
---|---|
rs10817988 | 0.86[ASN][1000 genomes] |
rs10983030 | 0.92[CEU][hapmap] |
rs10983447 | 0.95[EUR][1000 genomes] |
rs10983513 | 0.86[ASN][1000 genomes] |
rs10983546 | 0.84[ASN][1000 genomes] |
rs11792527 | 0.85[CHB][hapmap];0.86[JPT][hapmap];0.86[ASN][1000 genomes] |
rs12375515 | 0.86[ASN][1000 genomes] |
rs12379552 | 0.90[EUR][1000 genomes] |
rs1355599 | 0.92[ASN][1000 genomes] |
rs16923900 | 0.84[ASN][1000 genomes] |
rs1800975 | 0.92[CEU][hapmap];0.90[EUR][1000 genomes] |
rs2026132 | 0.92[CEU][hapmap] |
rs2036959 | 0.92[CEU][hapmap];0.98[EUR][1000 genomes] |
rs2668792 | 1.00[CEU][hapmap];0.99[EUR][1000 genomes] |
rs2668793 | 0.98[EUR][1000 genomes] |
rs2668798 | 0.95[EUR][1000 genomes] |
rs2773347 | 0.92[CEU][hapmap] |
rs2773351 | 0.92[CEU][hapmap] |
rs2805767 | 0.92[CEU][hapmap] |
rs2805777 | 0.92[CEU][hapmap] |
rs2805779 | 0.88[CEU][hapmap] |
rs2805824 | 1.00[CEU][hapmap];0.99[EUR][1000 genomes] |
rs2805825 | 0.99[EUR][1000 genomes] |
rs2805826 | 0.98[EUR][1000 genomes] |
rs2805827 | 0.92[ASN][1000 genomes] |
rs2805828 | 0.92[CEU][hapmap];0.92[EUR][1000 genomes] |
rs2805829 | 0.92[EUR][1000 genomes] |
rs2805832 | 0.89[EUR][1000 genomes] |
rs2805837 | 0.92[CEU][hapmap];0.87[EUR][1000 genomes] |
rs2805839 | 0.92[CEU][hapmap];0.81[EUR][1000 genomes] |
rs2805840 | 0.95[EUR][1000 genomes] |
rs2808668 | 0.92[CEU][hapmap];0.87[EUR][1000 genomes] |
rs2808672 | 0.85[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes] |
rs2808673 | 0.92[CEU][hapmap];0.92[EUR][1000 genomes] |
rs2808675 | 0.92[CEU][hapmap];0.92[EUR][1000 genomes] |
rs2808677 | 0.92[CEU][hapmap];0.93[EUR][1000 genomes] |
rs2808679 | 0.92[ASN][1000 genomes] |
rs2808680 | 0.92[ASN][1000 genomes] |
rs2808683 | 0.96[EUR][1000 genomes] |
rs2808685 | 0.98[EUR][1000 genomes] |
rs2808686 | 1.00[CEU][hapmap];0.98[EUR][1000 genomes] |
rs2808687 | 0.97[EUR][1000 genomes] |
rs2808689 | 0.99[EUR][1000 genomes] |
rs2808691 | 0.99[EUR][1000 genomes] |
rs2808694 | 0.85[EUR][1000 genomes] |
rs2808701 | 0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs2808703 | 0.87[EUR][1000 genomes] |
rs7849815 | 0.84[ASN][1000 genomes] |
rs953199 | 0.85[CHB][hapmap];0.80[JPT][hapmap];0.86[ASN][1000 genomes] |
rs958346 | 0.88[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv893610 | chr9:100324086-100496160 | Active TSS Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 32 gene(s) | inside rSNPs | diseases |
2 | nsv1043753 | chr9:100458109-100599265 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
3 | nsv614934 | chr9:100482976-100550253 | Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:100486800-100490600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr9:100489800-100490800 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |