Variant report
Variant | rs56923909 |
---|---|
Chromosome Location | chr7:80739612-80739613 |
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] |
---|---|
rs10243366 | 1.00[EUR][1000 genomes] |
rs10499866 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10499867 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10499868 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1406391 | 1.00[EUR][1000 genomes] |
rs16886939 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17154625 | 1.00[EUR][1000 genomes] |
rs17154734 | 1.00[EUR][1000 genomes] |
rs17154781 | 0.90[AMR][1000 genomes] |
rs17154789 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1881542 | 1.00[EUR][1000 genomes] |
rs2367107 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs3891959 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56661645 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56992458 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59232679 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59248712 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59283036 | 1.00[EUR][1000 genomes] |
rs59515047 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60302424 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61022986 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61242250 | 1.00[EUR][1000 genomes] |
rs6945017 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6947445 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6954567 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6954716 | 1.00[EUR][1000 genomes] |
rs6955012 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6955165 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6955495 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6978218 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6978720 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7780684 | 1.00[EUR][1000 genomes] |
rs7801407 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1034690 | chr7:80520004-80987682 | Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
2 | nsv888552 | chr7:80683308-80755310 | Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
3 | nsv888553 | chr7:80683308-80766407 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
4 | nsv888554 | chr7:80695828-80755310 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
5 | nsv888555 | chr7:80695828-80766407 | Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
6 | nsv888556 | chr7:80695828-80797794 | Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer | Chromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
7 | nsv831044 | chr7:80721773-80918591 | Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:80738400-80743400 | Enhancers | Primary hematopoietic stem cells short term culture | blood |
2 | chr7:80739400-80740800 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
3 | chr7:80739600-80740800 | Enhancers | A549 | lung |