Variant report
Variant | rs72697434 |
---|---|
Chromosome Location | chr9:17996255-17996256 |
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] |
---|---|
rs10756930 | 0.81[EUR][1000 genomes] |
rs10756931 | 0.81[EUR][1000 genomes] |
rs10810884 | 1.00[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs10810889 | 1.00[AFR][1000 genomes] |
rs10810890 | 0.87[EUR][1000 genomes] |
rs10810900 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs10810901 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs10963392 | 1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs10963412 | 0.87[EUR][1000 genomes] |
rs10963426 | 1.00[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs10963433 | 0.84[EUR][1000 genomes] |
rs10963439 | 1.00[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs10963440 | 1.00[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs10963445 | 1.00[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs10963447 | 1.00[AFR][1000 genomes] |
rs10963454 | 1.00[AFR][1000 genomes] |
rs10963455 | 1.00[AFR][1000 genomes] |
rs11532854 | 0.84[EUR][1000 genomes] |
rs12237150 | 1.00[AFR][1000 genomes] |
rs12238245 | 1.00[AFR][1000 genomes] |
rs12553148 | 1.00[AFR][1000 genomes];0.90[EUR][1000 genomes] |
rs12553925 | 0.90[EUR][1000 genomes] |
rs12554268 | 0.90[EUR][1000 genomes] |
rs12683106 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12685471 | 0.90[EUR][1000 genomes] |
rs12686274 | 0.81[EUR][1000 genomes] |
rs12686297 | 1.00[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs16936214 | 1.00[AFR][1000 genomes] |
rs16936263 | 0.90[EUR][1000 genomes] |
rs16936310 | 1.00[AFR][1000 genomes] |
rs1854579 | 0.87[EUR][1000 genomes] |
rs2026900 | 1.00[AFR][1000 genomes] |
rs2026901 | 1.00[AFR][1000 genomes] |
rs2210327 | 1.00[AFR][1000 genomes] |
rs58805966 | 1.00[AMR][1000 genomes] |
rs72697455 | 1.00[AFR][1000 genomes] |
rs72697457 | 1.00[AFR][1000 genomes] |
rs72697489 | 0.81[EUR][1000 genomes] |
rs72697491 | 0.84[EUR][1000 genomes] |
rs72699409 | 1.00[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv613706 | chr9:17718918-18090934 | Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | nsv613707 | chr9:17720175-18070475 | Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv613708 | chr9:17720175-18072085 | Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv892677 | chr9:17918806-18002205 | Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS | n/a | n/a | inside rSNPs | diseases |
5 | nsv1021862 | chr9:17931213-18052101 | Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv518330 | chr9:17965723-18017562 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | esv2752288 | chr9:17965723-18036892 | Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:17988200-18004400 | Weak transcription | Aorta | Aorta |
2 | chr9:17990600-17998000 | Enhancers | Hela-S3 | cervix |
3 | chr9:17993200-17997000 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
4 | chr9:17995200-18003400 | Weak transcription | Duodenum Mucosa | Duodenum |
5 | chr9:17995400-18002000 | Weak transcription | Duodenum Smooth Muscle | Duodenum |