Variant report
| Variant | rs6900044 |
|---|---|
| Chromosome Location | chr6:82176420-82176421 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:1 , 50 per page) page:
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| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr6:82174222..82177213-chr6:82462255..82464769,2 | MCF-7 | breast: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000112773 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:20)
| rs_ID | r2[population] |
|---|---|
| rs10943813 | 0.89[AFR][1000 genomes] |
| rs1145889 | 0.81[CEU][hapmap] |
| rs11964002 | 0.89[AFR][1000 genomes];0.82[ASN][1000 genomes] |
| rs11966310 | 0.89[AFR][1000 genomes];0.82[ASN][1000 genomes] |
| rs12213217 | 0.84[EUR][1000 genomes] |
| rs12213269 | 0.84[EUR][1000 genomes] |
| rs1276882 | 0.80[CEU][hapmap] |
| rs1321762 | 0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes] |
| rs1419030 | 0.86[CHB][hapmap] |
| rs17438648 | 0.87[AFR][1000 genomes];0.82[ASN][1000 genomes] |
| rs17529410 | 0.89[AFR][1000 genomes];0.82[ASN][1000 genomes] |
| rs4126327 | 0.84[EUR][1000 genomes] |
| rs58512216 | 0.89[AFR][1000 genomes];0.82[ASN][1000 genomes] |
| rs67524984 | 0.89[AFR][1000 genomes] |
| rs9350930 | 0.81[CEU][hapmap] |
| rs9353014 | 0.84[EUR][1000 genomes] |
| rs9359497 | 0.84[EUR][1000 genomes] |
| rs9443924 | 0.83[EUR][1000 genomes] |
| rs9449340 | 0.84[EUR][1000 genomes] |
| rs9449342 | 0.80[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv604087 | chr6:81792413-82326091 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
| 2 | nsv1032655 | chr6:81942397-82225830 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
| 3 | esv3475143 | chr6:82144215-82179186 | Enhancers Weak transcription Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
| 4 | esv3475144 | chr6:82144215-82179186 | Enhancers Weak transcription Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
| 5 | esv2624240 | chr6:82174953-82184774 | Inactive region | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
| 6 | esv19865 | chr6:82176187-82177524 | Inactive region | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
