Variant report
Variant | rs1181803 |
---|---|
Chromosome Location | chr7:124179535-124179536 |
allele | C/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] |
---|---|
rs10225755 | 0.83[EUR][1000 genomes] |
rs10236164 | 0.87[EUR][1000 genomes] |
rs10236310 | 0.87[EUR][1000 genomes] |
rs10259695 | 0.81[ASN][1000 genomes] |
rs10458294 | 0.81[EUR][1000 genomes] |
rs10954037 | 0.85[EUR][1000 genomes] |
rs1181804 | 0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1181805 | 0.85[EUR][1000 genomes] |
rs1181807 | 0.89[EUR][1000 genomes] |
rs12706607 | 0.86[EUR][1000 genomes] |
rs12706608 | 0.86[EUR][1000 genomes] |
rs12706609 | 0.86[EUR][1000 genomes] |
rs13243734 | 0.86[EUR][1000 genomes] |
rs17147239 | 0.87[EUR][1000 genomes] |
rs17394006 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs17472367 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs2159182 | 0.91[EUR][1000 genomes] |
rs2402732 | 0.86[EUR][1000 genomes] |
rs4568562 | 0.81[ASN][1000 genomes] |
rs4731191 | 0.87[EUR][1000 genomes] |
rs6948690 | 0.86[EUR][1000 genomes] |
rs6968639 | 0.86[EUR][1000 genomes] |
rs73219044 | 0.81[EUR][1000 genomes] |
rs7777394 | 0.88[EUR][1000 genomes] |
rs7777417 | 0.87[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv1795113 | chr7:123885477-124188665 | Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv429809 | chr7:123937674-124835925 | Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 49 gene(s) | inside rSNPs | diseases |
3 | esv1808414 | chr7:123957376-124188665 | Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv525687 | chr7:124138187-124196444 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | nsv608340 | chr7:124138187-124196444 | Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
6 | nsv831118 | chr7:124172267-124347527 | Enhancers Active TSS Weak transcription Flanking 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 | chr7:124177000-124181800 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
2 | chr7:124179200-124179800 | Enhancers | Fetal Lung | lung |