Variant report
Variant | rs55838720 |
---|---|
Chromosome Location | chr9:104350072-104350073 |
allele | C/T |
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] |
---|---|
rs10512283 | 0.82[EUR][1000 genomes] |
rs10512284 | 0.82[EUR][1000 genomes] |
rs10819954 | 0.82[EUR][1000 genomes] |
rs10819955 | 0.82[EUR][1000 genomes] |
rs10819956 | 0.82[EUR][1000 genomes] |
rs10819958 | 0.82[EUR][1000 genomes] |
rs10819959 | 0.82[EUR][1000 genomes] |
rs10819961 | 0.82[EUR][1000 genomes] |
rs10989572 | 0.82[EUR][1000 genomes] |
rs10989592 | 0.81[EUR][1000 genomes] |
rs12708308 | 0.80[EUR][1000 genomes] |
rs1323427 | 0.82[EUR][1000 genomes] |
rs13289501 | 0.82[EUR][1000 genomes] |
rs1407873 | 0.82[EUR][1000 genomes] |
rs1407874 | 0.82[EUR][1000 genomes] |
rs17189275 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs17189562 | 0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs17189604 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs17189821 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs17197124 | 0.82[EUR][1000 genomes] |
rs17774987 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs1853447 | 0.82[EUR][1000 genomes] |
rs34888126 | 0.92[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs35227408 | 0.82[EUR][1000 genomes] |
rs35569161 | 0.92[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs4266702 | 0.82[EUR][1000 genomes] |
rs4442195 | 0.82[EUR][1000 genomes] |
rs55731515 | 0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs55749212 | 0.88[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs56052939 | 0.92[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs56073506 | 0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs56246731 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs58830774 | 0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs6479060 | 0.81[EUR][1000 genomes] |
rs72745350 | 0.87[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs72745355 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1046975 | chr9:104167583-104659873 | Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 15 gene(s) | inside rSNPs | diseases |
2 | nsv949579 | chr9:104229820-104512923 | Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 14 gene(s) | inside rSNPs | diseases |
3 | nsv1052492 | chr9:104263419-104387782 | Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
4 | nsv831672 | chr9:104300755-104480849 | Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:104345400-104352000 | Weak transcription | A549 | lung |
2 | chr9:104349600-104350200 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
3 | chr9:104350000-104350600 | Enhancers | HSMMtube | muscle |