Variant report
Variant | rs4340718 |
---|---|
Chromosome Location | chr3:161768924-161768925 |
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] |
---|---|
rs1027921 | 0.84[EUR][1000 genomes] |
rs1119974 | 0.83[EUR][1000 genomes] |
rs12696134 | 0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1355290 | 0.82[EUR][1000 genomes] |
rs1397238 | 0.84[EUR][1000 genomes] |
rs1397239 | 0.84[EUR][1000 genomes] |
rs1510346 | 0.84[EUR][1000 genomes] |
rs1813301 | 0.85[EUR][1000 genomes] |
rs2089737 | 0.85[EUR][1000 genomes] |
rs2136712 | 0.84[EUR][1000 genomes] |
rs2175265 | 0.84[EUR][1000 genomes] |
rs4241434 | 0.82[EUR][1000 genomes] |
rs4312667 | 0.82[EUR][1000 genomes] |
rs4602407 | 0.82[EUR][1000 genomes] |
rs4856668 | 0.85[EUR][1000 genomes] |
rs4856743 | 0.82[EUR][1000 genomes] |
rs6789187 | 0.85[EUR][1000 genomes] |
rs6789851 | 0.85[EUR][1000 genomes] |
rs7635026 | 0.82[EUR][1000 genomes] |
rs9816747 | 0.84[EUR][1000 genomes] |
rs9819461 | 0.84[EUR][1000 genomes] |
rs9876455 | 0.85[EUR][1000 genomes] |
rs9882103 | 0.81[EUR][1000 genomes] |
rs9883680 | 0.85[EUR][1000 genomes] |
rs993596 | 0.81[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv533237 | chr3:161019834-161804660 | Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 91 gene(s) | inside rSNPs | diseases |
2 | nsv460918 | chr3:161754109-161791399 | Enhancers Weak transcription Active TSS ZNF genes & repeats | n/a | n/a | inside rSNPs | diseases |
3 | nsv592143 | chr3:161754109-161791399 | Enhancers Weak transcription Active TSS ZNF genes & repeats | n/a | n/a | inside rSNPs | diseases |
4 | esv2034625 | chr3:161768909-161769333 | Weak transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:161766600-161771000 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
2 | chr3:161768000-161769000 | Enhancers | iPS-18 Cell Line | embryonic stem cell |