Variant report
Variant | rs6837235 |
---|---|
Chromosome Location | chr4:21875235-21875236 |
allele | A/C |
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] |
---|---|
rs1040039 | 0.89[ASN][1000 genomes] |
rs10516400 | 0.84[ASN][1000 genomes] |
rs10516407 | 0.83[ASN][1000 genomes] |
rs10805230 | 0.87[ASN][1000 genomes] |
rs10938854 | 0.81[ASN][1000 genomes] |
rs10938860 | 0.89[ASN][1000 genomes] |
rs11723231 | 0.84[ASN][1000 genomes] |
rs11725506 | 0.89[ASN][1000 genomes] |
rs11728958 | 0.84[ASN][1000 genomes] |
rs11731098 | 0.87[ASN][1000 genomes] |
rs11732527 | 0.83[ASN][1000 genomes] |
rs11734604 | 0.81[ASN][1000 genomes] |
rs11736882 | 0.81[ASN][1000 genomes] |
rs11931923 | 0.87[ASN][1000 genomes] |
rs11938269 | 0.81[ASN][1000 genomes] |
rs12503772 | 0.84[ASN][1000 genomes] |
rs12512545 | 0.91[ASN][1000 genomes] |
rs12512603 | 0.91[ASN][1000 genomes] |
rs13104527 | 0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs13105122 | 0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs13105154 | 0.81[ASN][1000 genomes] |
rs13110177 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs13112610 | 0.89[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs13119994 | 0.84[ASN][1000 genomes] |
rs13128189 | 0.84[ASN][1000 genomes] |
rs13129819 | 0.89[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs13132296 | 0.81[ASN][1000 genomes] |
rs13135188 | 0.81[ASN][1000 genomes] |
rs13135698 | 0.81[ASN][1000 genomes] |
rs13141904 | 0.81[ASN][1000 genomes] |
rs13142511 | 0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1398835 | 0.81[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs1459279 | 0.84[ASN][1000 genomes] |
rs1459280 | 0.84[ASN][1000 genomes] |
rs168626 | 0.87[ASN][1000 genomes] |
rs17498614 | 0.81[ASN][1000 genomes] |
rs17564865 | 0.81[ASN][1000 genomes] |
rs17566434 | 0.84[ASN][1000 genomes] |
rs17570050 | 0.81[ASN][1000 genomes] |
rs17570140 | 0.83[ASN][1000 genomes] |
rs1841187 | 0.84[ASN][1000 genomes] |
rs1841188 | 0.84[ASN][1000 genomes] |
rs184860 | 0.81[ASN][1000 genomes] |
rs2137650 | 0.87[ASN][1000 genomes] |
rs2175779 | 0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs2175780 | 0.89[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs2323128 | 0.87[ASN][1000 genomes] |
rs34008037 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs34375823 | 0.81[ASN][1000 genomes] |
rs34708714 | 0.84[ASN][1000 genomes] |
rs34839938 | 0.87[ASN][1000 genomes] |
rs35146316 | 0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs35161937 | 0.81[ASN][1000 genomes] |
rs35175333 | 0.84[ASN][1000 genomes] |
rs35215732 | 0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs35489277 | 0.83[ASN][1000 genomes] |
rs35711081 | 0.83[ASN][1000 genomes] |
rs35719625 | 0.83[ASN][1000 genomes] |
rs35733545 | 0.81[ASN][1000 genomes] |
rs35827665 | 0.87[ASN][1000 genomes] |
rs35921228 | 0.84[ASN][1000 genomes] |
rs35937671 | 0.84[ASN][1000 genomes] |
rs360698 | 0.87[ASN][1000 genomes] |
rs4443267 | 0.83[ASN][1000 genomes] |
rs4455402 | 0.87[ASN][1000 genomes] |
rs4618303 | 0.84[ASN][1000 genomes] |
rs4631029 | 0.84[ASN][1000 genomes] |
rs4696989 | 0.86[ASN][1000 genomes] |
rs4697243 | 0.89[ASN][1000 genomes] |
rs57134420 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs57505034 | 0.84[ASN][1000 genomes] |
rs60627982 | 0.88[AFR][1000 genomes] |
rs6448076 | 0.81[ASN][1000 genomes] |
rs6448091 | 0.84[ASN][1000 genomes] |
rs6814698 | 0.89[ASN][1000 genomes] |
rs6819627 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6823352 | 0.83[ASN][1000 genomes] |
rs6830224 | 0.91[ASN][1000 genomes] |
rs6834778 | 0.81[ASN][1000 genomes] |
rs6839725 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6839776 | 1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6852952 | 0.89[ASN][1000 genomes] |
rs6853293 | 0.89[ASN][1000 genomes] |
rs71607091 | 0.81[ASN][1000 genomes] |
rs71607093 | 0.84[ASN][1000 genomes] |
rs71607096 | 0.87[ASN][1000 genomes] |
rs7656546 | 0.84[ASN][1000 genomes] |
rs7659552 | 0.83[ASN][1000 genomes] |
rs7662958 | 0.81[ASN][1000 genomes] |
rs7695756 | 0.81[ASN][1000 genomes] |
rs9884203 | 0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs9884843 | 0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs9995230 | 0.84[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv817467 | chr4:21602921-22422816 | Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | esv2757924 | chr4:21873204-21980559 | Bivalent/Poised TSS Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | esv2759231 | chr4:21873204-21980559 | Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv428440 | chr4:21873204-21980559 | Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:21874000-21875600 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
2 | chr4:21874400-21879200 | Weak transcription | Fetal Heart | heart |
3 | chr4:21874600-21875600 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
4 | chr4:21874600-21876000 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
5 | chr4:21874800-21875800 | Enhancers | Muscle Satellite Cultured Cells | -- |
6 | chr4:21875000-21875600 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
7 | chr4:21875200-21875400 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |