Variant report
Variant | rs17092648 |
---|---|
Chromosome Location | chr8:20355313-20355314 |
allele | A/G |
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] |
---|---|
rs10112289 | 1.00[EUR][1000 genomes] |
rs1026962 | 1.00[EUR][1000 genomes] |
rs12114223 | 1.00[EUR][1000 genomes] |
rs17092285 | 1.00[EUR][1000 genomes] |
rs17092525 | 1.00[EUR][1000 genomes] |
rs17116648 | 1.00[EUR][1000 genomes] |
rs4330706 | 1.00[EUR][1000 genomes] |
rs57350066 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs58021006 | 0.92[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs60949054 | 1.00[EUR][1000 genomes] |
rs60973888 | 1.00[EUR][1000 genomes] |
rs67850346 | 0.81[AFR][1000 genomes] |
rs6993881 | 1.00[EUR][1000 genomes] |
rs7003050 | 1.00[EUR][1000 genomes] |
rs7004136 | 1.00[EUR][1000 genomes] |
rs7012806 | 1.00[EUR][1000 genomes] |
rs7015313 | 1.00[EUR][1000 genomes] |
rs7017244 | 1.00[EUR][1000 genomes] |
rs7017444 | 1.00[EUR][1000 genomes] |
rs7018201 | 1.00[EUR][1000 genomes] |
rs73607619 | 1.00[EUR][1000 genomes] |
rs73607621 | 1.00[EUR][1000 genomes] |
rs73607627 | 1.00[EUR][1000 genomes] |
rs73607631 | 0.84[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73607698 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73609138 | 1.00[EUR][1000 genomes] |
rs73609140 | 1.00[EUR][1000 genomes] |
rs73609141 | 1.00[EUR][1000 genomes] |
rs73609174 | 1.00[EUR][1000 genomes] |
rs73617815 | 1.00[EUR][1000 genomes] |
rs7459906 | 1.00[EUR][1000 genomes] |
rs7813418 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1033511 | chr8:19751299-20625091 | Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 17 gene(s) | inside rSNPs | diseases |
2 | nsv530877 | chr8:19873053-20593254 | Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
3 | esv2758152 | chr8:20228949-20514807 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | esv2759603 | chr8:20228949-20514807 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv469890 | chr8:20239114-20445136 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
6 | nsv482881 | chr8:20239114-20445136 | Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
7 | nsv916454 | chr8:20342959-20531705 | Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:20353400-20363800 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
2 | chr8:20353800-20358000 | Weak transcription | Primary T cells from cord blood | blood |
3 | chr8:20355000-20355600 | Enhancers | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
4 | chr8:20355200-20355600 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |