Variant report
Variant | rs4896508 |
---|---|
Chromosome Location | chr6:140647506-140647507 |
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] |
---|---|
rs11155107 | 0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs1119397 | 0.87[ASN][1000 genomes] |
rs1121833 | 0.92[ASN][1000 genomes] |
rs12055615 | 0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12174980 | 0.86[ASN][1000 genomes] |
rs12660474 | 0.90[ASN][1000 genomes] |
rs12660560 | 0.84[ASN][1000 genomes] |
rs12661752 | 0.81[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12662046 | 0.90[ASN][1000 genomes] |
rs12662151 | 0.81[ASN][1000 genomes] |
rs12662848 | 0.93[ASN][1000 genomes] |
rs12663424 | 0.94[ASN][1000 genomes] |
rs12663444 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12663480 | 0.86[ASN][1000 genomes] |
rs12665797 | 0.90[ASN][1000 genomes] |
rs13191189 | 0.84[ASN][1000 genomes] |
rs13192756 | 0.82[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs13194271 | 0.94[ASN][1000 genomes] |
rs13204703 | 0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs13207048 | 0.87[ASN][1000 genomes] |
rs13208097 | 0.94[ASN][1000 genomes] |
rs13213875 | 0.82[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs13214458 | 0.83[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1496110 | 0.90[ASN][1000 genomes] |
rs1496112 | 0.87[ASN][1000 genomes] |
rs1496113 | 0.86[ASN][1000 genomes] |
rs1519592 | 0.87[ASN][1000 genomes] |
rs1587171 | 0.86[ASN][1000 genomes] |
rs1603348 | 0.86[ASN][1000 genomes] |
rs1603349 | 0.86[ASN][1000 genomes] |
rs17053906 | 0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs17069852 | 0.86[ASN][1000 genomes] |
rs17069854 | 0.86[ASN][1000 genomes] |
rs17192 | 0.92[ASN][1000 genomes] |
rs1856752 | 0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2020197 | 0.82[ASN][1000 genomes] |
rs2050135 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2103669 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2328062 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs34358600 | 0.82[ASN][1000 genomes] |
rs34753441 | 0.86[ASN][1000 genomes] |
rs34858573 | 0.82[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs34984534 | 0.86[ASN][1000 genomes] |
rs35465283 | 0.86[ASN][1000 genomes] |
rs35626395 | 0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs35686278 | 0.88[ASN][1000 genomes] |
rs36074095 | 0.86[ASN][1000 genomes] |
rs4323321 | 0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs4391280 | 0.83[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs4562159 | 0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4637665 | 0.87[ASN][1000 genomes] |
rs477498 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4896509 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs520322 | 0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs533610 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs57291519 | 0.86[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs62431097 | 0.82[ASN][1000 genomes] |
rs62431100 | 0.82[ASN][1000 genomes] |
rs62431101 | 0.83[ASN][1000 genomes] |
rs66460448 | 0.81[ASN][1000 genomes] |
rs71562538 | 0.84[ASN][1000 genomes] |
rs7758187 | 0.84[ASN][1000 genomes] |
rs7761894 | 0.82[ASN][1000 genomes] |
rs9321765 | 0.90[ASN][1000 genomes] |
rs9321769 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9373258 | 0.82[ASN][1000 genomes] |
rs9373259 | 0.84[ASN][1000 genomes] |
rs9373260 | 0.86[ASN][1000 genomes] |
rs9373261 | 0.86[ASN][1000 genomes] |
rs9373262 | 0.87[ASN][1000 genomes] |
rs9373266 | 0.90[ASN][1000 genomes] |
rs9373267 | 0.88[ASN][1000 genomes] |
rs9373269 | 0.92[ASN][1000 genomes] |
rs9373270 | 0.92[ASN][1000 genomes] |
rs9373272 | 0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9373273 | 0.86[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs9373274 | 0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs9373276 | 0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs9373278 | 0.83[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9376497 | 0.82[ASN][1000 genomes] |
rs9376498 | 0.82[ASN][1000 genomes] |
rs9376502 | 0.86[ASN][1000 genomes] |
rs9376503 | 0.86[ASN][1000 genomes] |
rs9376504 | 0.86[ASN][1000 genomes] |
rs9376506 | 0.90[ASN][1000 genomes] |
rs9376511 | 0.92[ASN][1000 genomes] |
rs9376512 | 0.92[ASN][1000 genomes] |
rs9376518 | 0.83[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9385899 | 0.81[ASN][1000 genomes] |
rs9385900 | 0.82[ASN][1000 genomes] |
rs9385901 | 0.84[ASN][1000 genomes] |
rs9385902 | 0.84[ASN][1000 genomes] |
rs9385903 | 0.86[ASN][1000 genomes] |
rs9385906 | 0.87[ASN][1000 genomes] |
rs9385908 | 0.94[ASN][1000 genomes] |
rs9389749 | 0.82[ASN][1000 genomes] |
rs9389750 | 0.82[ASN][1000 genomes] |
rs9389751 | 0.84[ASN][1000 genomes] |
rs9389753 | 0.86[ASN][1000 genomes] |
rs9389754 | 0.86[ASN][1000 genomes] |
rs9389755 | 0.86[ASN][1000 genomes] |
rs9389757 | 0.86[ASN][1000 genomes] |
rs9389760 | 0.86[ASN][1000 genomes] |
rs9389763 | 0.86[ASN][1000 genomes] |
rs9389767 | 0.86[ASN][1000 genomes] |
rs9389768 | 0.87[ASN][1000 genomes] |
rs9389772 | 0.90[ASN][1000 genomes] |
rs9389773 | 0.88[ASN][1000 genomes] |
rs9389774 | 0.85[ASN][1000 genomes] |
rs9389776 | 0.86[ASN][1000 genomes] |
rs9389777 | 0.87[ASN][1000 genomes] |
rs9389780 | 0.90[ASN][1000 genomes] |
rs9389781 | 0.90[ASN][1000 genomes] |
rs9389782 | 0.88[ASN][1000 genomes] |
rs9389783 | 0.90[ASN][1000 genomes] |
rs9389784 | 0.92[ASN][1000 genomes] |
rs9389785 | 0.92[ASN][1000 genomes] |
rs9389789 | 0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9389793 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs9389794 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs9399308 | 0.82[ASN][1000 genomes] |
rs9399310 | 0.87[ASN][1000 genomes] |
rs9399315 | 0.83[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9399316 | 0.83[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs9403148 | 0.84[ASN][1000 genomes] |
rs9403149 | 0.81[ASN][1000 genomes] |
rs9403150 | 0.86[ASN][1000 genomes] |
rs9403151 | 0.86[ASN][1000 genomes] |
rs9403153 | 0.86[ASN][1000 genomes] |
rs9403155 | 0.86[ASN][1000 genomes] |
rs9403156 | 0.86[ASN][1000 genomes] |
rs9403157 | 0.86[ASN][1000 genomes] |
rs9403159 | 0.87[ASN][1000 genomes] |
rs9403165 | 0.86[ASN][1000 genomes] |
rs9403168 | 0.88[ASN][1000 genomes] |
rs9403170 | 0.90[ASN][1000 genomes] |
rs9403171 | 0.92[ASN][1000 genomes] |
rs9403173 | 0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs9403174 | 0.83[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9403176 | 0.83[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9403177 | 0.83[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9484347 | 0.84[ASN][1000 genomes] |
rs9791338 | 0.87[ASN][1000 genomes] |
rs997388 | 0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1016532 | chr6:140174639-141029988 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 17 gene(s) | inside rSNPs | diseases |
2 | nsv1015293 | chr6:140544956-140798437 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | nsv817390 | chr6:140558103-141166039 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:140641400-140658000 | Weak transcription | K562 | blood |
2 | chr6:140643200-140650800 | Weak transcription | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
3 | chr6:140647200-140647600 | ZNF genes & repeats | Aorta | Aorta |
4 | chr6:140647400-140649000 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |