Variant report
Variant | rs73290680 |
---|---|
Chromosome Location | chr7:25501950-25501951 |
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] |
---|---|
rs11978553 | 1.00[EUR][1000 genomes] |
rs11980207 | 1.00[EUR][1000 genomes] |
rs11980890 | 1.00[EUR][1000 genomes] |
rs12112715 | 1.00[EUR][1000 genomes] |
rs17151642 | 1.00[EUR][1000 genomes] |
rs17151705 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs28507884 | 1.00[EUR][1000 genomes] |
rs28530564 | 1.00[EUR][1000 genomes] |
rs55666498 | 1.00[EUR][1000 genomes] |
rs55800607 | 1.00[EUR][1000 genomes] |
rs56914684 | 1.00[EUR][1000 genomes] |
rs57244176 | 1.00[EUR][1000 genomes] |
rs57404942 | 1.00[EUR][1000 genomes] |
rs58446425 | 1.00[EUR][1000 genomes] |
rs6956001 | 1.00[EUR][1000 genomes] |
rs73290683 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73691547 | 1.00[EUR][1000 genomes] |
rs73691556 | 1.00[EUR][1000 genomes] |
rs73691559 | 1.00[EUR][1000 genomes] |
rs73691560 | 1.00[EUR][1000 genomes] |
rs73691561 | 1.00[EUR][1000 genomes] |
rs73691563 | 1.00[EUR][1000 genomes] |
rs73691564 | 1.00[EUR][1000 genomes] |
rs73691569 | 1.00[EUR][1000 genomes] |
rs73691573 | 1.00[EUR][1000 genomes] |
rs73691587 | 1.00[EUR][1000 genomes] |
rs73691588 | 1.00[EUR][1000 genomes] |
rs73691593 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv606426 | chr7:25254125-25621579 | Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
2 | nsv1016813 | chr7:25405859-26150509 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 108 gene(s) | inside rSNPs | diseases |
3 | nsv538803 | chr7:25405859-26150509 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 108 gene(s) | inside rSNPs | diseases |
4 | nsv1033664 | chr7:25471881-25503391 | Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | nsv1033757 | chr7:25472222-25504421 | Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:25499000-25523800 | Weak transcription | Gastric | stomach |