Variant report
Variant | rs12692740 |
---|---|
Chromosome Location | chr2:151369593-151369594 |
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] |
---|---|
rs10177711 | 0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs10803791 | 0.85[ASN][1000 genomes] |
rs10930130 | 0.84[ASN][1000 genomes] |
rs12692718 | 0.85[ASN][1000 genomes] |
rs12692720 | 0.85[ASN][1000 genomes] |
rs12692722 | 0.85[ASN][1000 genomes] |
rs12692729 | 0.97[ASN][1000 genomes] |
rs12692739 | 0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12692747 | 0.85[ASN][1000 genomes] |
rs12692748 | 0.82[AMR][1000 genomes];0.96[ASN][1000 genomes] |
rs13011088 | 0.86[ASN][1000 genomes] |
rs13012155 | 0.85[ASN][1000 genomes] |
rs1569158 | 0.85[ASN][1000 genomes] |
rs1609302 | 0.83[ASN][1000 genomes] |
rs1852688 | 0.84[ASN][1000 genomes] |
rs1852689 | 0.86[ASN][1000 genomes] |
rs1919142 | 0.89[ASN][1000 genomes] |
rs2222760 | 0.92[ASN][1000 genomes] |
rs6432778 | 0.82[ASN][1000 genomes] |
rs6432779 | 0.82[ASN][1000 genomes] |
rs6432791 | 0.89[ASN][1000 genomes] |
rs6721757 | 0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6722263 | 0.82[ASN][1000 genomes] |
rs6735265 | 0.82[ASN][1000 genomes] |
rs6757626 | 0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72865991 | 0.99[ASN][1000 genomes] |
rs7561737 | 0.85[ASN][1000 genomes] |
rs7586782 | 0.86[ASN][1000 genomes] |
rs7600506 | 0.86[ASN][1000 genomes] |
rs7603369 | 0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7603608 | 0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7605020 | 0.89[ASN][1000 genomes] |
rs7609510 | 0.86[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1001838 | chr2:150819672-151745876 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 51 gene(s) | inside rSNPs | diseases |
2 | nsv535980 | chr2:150819672-151745876 | Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 51 gene(s) | inside rSNPs | diseases |
3 | nsv532473 | chr2:151164210-151701860 | Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
4 | nsv834414 | chr2:151209374-151413309 | Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 29 gene(s) | inside rSNPs | diseases |
5 | nsv1001777 | chr2:151351927-151395620 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
6 | esv2762286 | chr2:151351927-151395632 | Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:151365400-151369600 | Weak transcription | NHLF | lung |
2 | chr2:151369400-151371400 | Enhancers | IMR90 fetal lung fibroblasts Cell Line | lung |