Variant report
Variant | rs7830125 |
---|---|
Chromosome Location | chr8:20290399-20290400 |
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] |
---|---|
rs1016646 | 1.00[AFR][1000 genomes] |
rs10464996 | 1.00[AFR][1000 genomes] |
rs10503682 | 1.00[AFR][1000 genomes] |
rs12056831 | 1.00[AFR][1000 genomes];0.88[EUR][1000 genomes] |
rs1383248 | 1.00[AFR][1000 genomes] |
rs17092359 | 0.81[EUR][1000 genomes] |
rs17092374 | 1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs17092434 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs17092492 | 0.82[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs17092502 | 0.82[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs17092511 | 0.82[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs17092733 | 1.00[AFR][1000 genomes] |
rs17412582 | 1.00[AFR][1000 genomes] |
rs17412734 | 1.00[AFR][1000 genomes] |
rs17412740 | 1.00[AFR][1000 genomes] |
rs17419795 | 1.00[AFR][1000 genomes] |
rs17420434 | 1.00[AFR][1000 genomes] |
rs17420455 | 1.00[AFR][1000 genomes] |
rs17490805 | 1.00[AFR][1000 genomes] |
rs17490847 | 1.00[AFR][1000 genomes] |
rs17491153 | 1.00[AFR][1000 genomes] |
rs17492344 | 1.00[AFR][1000 genomes] |
rs1979430 | 1.00[AFR][1000 genomes] |
rs1979431 | 1.00[AFR][1000 genomes] |
rs1979432 | 1.00[AFR][1000 genomes] |
rs2005365 | 1.00[AFR][1000 genomes] |
rs2086886 | 1.00[AFR][1000 genomes] |
rs2170171 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs2170172 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs35673104 | 1.00[AFR][1000 genomes] |
rs4430109 | 0.81[EUR][1000 genomes] |
rs4430110 | 0.81[EUR][1000 genomes] |
rs4430111 | 0.81[EUR][1000 genomes] |
rs4506236 | 0.86[EUR][1000 genomes] |
rs4576439 | 0.81[EUR][1000 genomes] |
rs4601325 | 1.00[AFR][1000 genomes] |
rs4610764 | 1.00[AFR][1000 genomes] |
rs4921708 | 1.00[AFR][1000 genomes] |
rs4921713 | 1.00[AFR][1000 genomes] |
rs4921718 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs4922161 | 1.00[AFR][1000 genomes] |
rs4922175 | 1.00[AFR][1000 genomes] |
rs4922177 | 1.00[AFR][1000 genomes] |
rs4922178 | 1.00[AFR][1000 genomes] |
rs4922179 | 1.00[AFR][1000 genomes] |
rs4922180 | 1.00[AFR][1000 genomes] |
rs4922181 | 1.00[AFR][1000 genomes] |
rs4922182 | 1.00[AFR][1000 genomes] |
rs4922183 | 1.00[AFR][1000 genomes] |
rs4922187 | 1.00[AFR][1000 genomes] |
rs4922189 | 1.00[AFR][1000 genomes] |
rs4922194 | 1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4922195 | 1.00[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs4922196 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs4922200 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs4922210 | 1.00[AFR][1000 genomes] |
rs56157706 | 1.00[AFR][1000 genomes] |
rs56171374 | 1.00[AFR][1000 genomes] |
rs58204896 | 1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs58247975 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs58430710 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs59876773 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs60888624 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs6586910 | 1.00[AFR][1000 genomes] |
rs6989281 | 1.00[AFR][1000 genomes] |
rs6994255 | 1.00[AFR][1000 genomes] |
rs6999584 | 1.00[AFR][1000 genomes] |
rs6999736 | 1.00[AFR][1000 genomes] |
rs7003097 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs73609155 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs73609159 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs7465534 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7827108 | 0.81[EUR][1000 genomes] |
rs7827252 | 0.90[EUR][1000 genomes] |
rs7827262 | 0.90[EUR][1000 genomes] |
rs950511 | 1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs999746 | 1.00[AMR][1000 genomes];0.90[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 | nsv831256 | chr8:20162233-20300224 | Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | 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 |
5 | 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 |
6 | 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 |
7 | 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 |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:20280000-20291800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr8:20283200-20293000 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
3 | chr8:20287200-20292000 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
4 | chr8:20289600-20292600 | Weak transcription | Stomach Mucosa | stomach |