Variant report
| Variant | rs73760853 |
|---|---|
| Chromosome Location | chr6:100775068-100775069 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:6)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:6 , 50 per page) page:
1
| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr6:100774621..100775576-chr6:101105387..101106278,3 | MCF-7 | breast: | |
| 2 | chr6:100774927..100775901-chr6:100927025..100927714,2 | MCF-7 | breast: | |
| 3 | chr6:100624189..100625158-chr6:100774800..100775571,3 | MCF-7 | breast: | |
| 4 | chr6:100623896..100624751-chr6:100774944..100775548,2 | MCF-7 | breast: | |
| 5 | chr6:100774639..100776281-chr6:100926982..100927977,6 | MCF-7 | breast: | |
| 6 | chr6:100774579..100775648-chr6:101105264..101106241,7 | MCF-7 | breast: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000216378 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:25)
| rs_ID | r2[population] |
|---|---|
| rs11962725 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs11964322 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs55692601 | 1.00[AMR][1000 genomes] |
| rs56176715 | 1.00[AMR][1000 genomes] |
| rs56876848 | 1.00[AMR][1000 genomes] |
| rs57185278 | 1.00[EUR][1000 genomes] |
| rs57335321 | 1.00[AMR][1000 genomes] |
| rs59301700 | 1.00[AMR][1000 genomes] |
| rs60973981 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73760809 | 1.00[AMR][1000 genomes] |
| rs73760820 | 1.00[AMR][1000 genomes] |
| rs73760821 | 1.00[AMR][1000 genomes] |
| rs73760822 | 1.00[AMR][1000 genomes] |
| rs73760824 | 1.00[AMR][1000 genomes] |
| rs73760825 | 1.00[AMR][1000 genomes] |
| rs73760826 | 1.00[AMR][1000 genomes] |
| rs73760828 | 1.00[AMR][1000 genomes] |
| rs73760831 | 1.00[AMR][1000 genomes] |
| rs73760862 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73760864 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73760865 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73760866 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs73760870 | 1.00[AMR][1000 genomes] |
| rs7749843 | 1.00[EUR][1000 genomes] |
| rs7771007 | 1.00[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv949535 | chr6:100740293-101469052 | Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
| 2 | nsv1028122 | chr6:100774245-100964347 | Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 5 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
