Variant report
| Variant | rs73609058 |
|---|---|
| Chromosome Location | chr6:149621237-149621238 |
| allele | C/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 | chr6:149617752..149621421-chr6:149622523..149625158,3 | K562 | blood: | |
| 2 | chr6:149621198..149623751-chr6:149635506..149639133,3 | MCF-7 | breast: | |
| 3 | chr6:149619314..149622625-chr6:149634430..149636159,3 | K562 | blood: | |
| 4 | chr6:149620609..149622948-chr6:149640554..149642656,2 | K562 | blood: | |
| 5 | chr6:149617347..149620525-chr6:149621010..149624915,3 | MCF-7 | breast: | |
| 6 | chr6:149618848..149621708-chr6:149625417..149626920,2 | K562 | blood: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000055208 | Chromatin interaction |
| ENSG00000216265 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:6)
| rs_ID | r2[population] |
|---|---|
| rs60038742 | 1.00[AMR][1000 genomes] |
| rs6911686 | 1.00[AMR][1000 genomes] |
| rs6911796 | 1.00[AMR][1000 genomes] |
| rs73607369 | 0.82[AFR][1000 genomes] |
| rs73609050 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs7752334 | 0.86[AFR][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 | nsv1024776 | chr6:149398652-149654593 | Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
| 2 | nsv1015360 | chr6:149609804-149649982 | Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
