Variant report
| Variant | rs485825 |
|---|---|
| Chromosome Location | chr7:80830951-80830952 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:4)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:4 , 50 per page) page:
1
| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr7:80821320..80824042-chr7:80830231..80831994,2 | MCF-7 | breast: | |
| 2 | chr7:80819982..80822822-chr7:80829998..80832398,2 | MCF-7 | breast: | |
| 3 | chr7:80548873..80550374-chr7:80829934..80832081,2 | MCF-7 | breast: | |
| 4 | chr7:80828235..80830977-chr7:80837024..80839340,2 | K562 | blood: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000226671 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:18)
| rs_ID | r2[population] |
|---|---|
| rs17628572 | 1.00[ASN][1000 genomes] |
| rs327682 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs327685 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs327687 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs327690 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs327691 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs327695 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs327696 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs327697 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs327709 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes] |
| rs471783 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs492377 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs500454 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs512906 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs517609 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs551994 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs7455610 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs996720 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page:
1
| 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 | 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 |
| 3 | nsv888557 | chr7:80813081-80917148 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
| 4 | nsv1023149 | chr7:80817550-80928090 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
