Variant report
| Variant | rs73749169 |
|---|---|
| Chromosome Location | chr6:82203107-82203108 |
| allele | C/G |
| 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:
1
| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr15:45003689..45005679-chr6:82202647..82204263,2 | K562 | blood: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000166710 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:33)
| rs_ID | r2[population] |
|---|---|
| rs55765987 | 1.00[AFR][1000 genomes] |
| rs55853385 | 1.00[AFR][1000 genomes] |
| rs55896603 | 1.00[AFR][1000 genomes] |
| rs55908447 | 1.00[AFR][1000 genomes] |
| rs55941921 | 0.87[AFR][1000 genomes] |
| rs56307420 | 1.00[AFR][1000 genomes] |
| rs56395455 | 0.87[AFR][1000 genomes] |
| rs57855828 | 1.00[AFR][1000 genomes] |
| rs58497319 | 1.00[AFR][1000 genomes] |
| rs59174879 | 1.00[AFR][1000 genomes] |
| rs59374553 | 1.00[AFR][1000 genomes] |
| rs60451676 | 1.00[AFR][1000 genomes] |
| rs60862286 | 1.00[AFR][1000 genomes] |
| rs60903961 | 1.00[AFR][1000 genomes] |
| rs73749143 | 1.00[AFR][1000 genomes] |
| rs73749144 | 1.00[AFR][1000 genomes] |
| rs73749145 | 1.00[AFR][1000 genomes] |
| rs73749147 | 1.00[AFR][1000 genomes] |
| rs73749155 | 1.00[AFR][1000 genomes] |
| rs73749156 | 1.00[AFR][1000 genomes] |
| rs73749157 | 1.00[AFR][1000 genomes] |
| rs73749158 | 1.00[AFR][1000 genomes] |
| rs73749159 | 1.00[AFR][1000 genomes] |
| rs73749160 | 1.00[AFR][1000 genomes] |
| rs73749161 | 1.00[AFR][1000 genomes] |
| rs73749162 | 1.00[AFR][1000 genomes] |
| rs73749163 | 1.00[AFR][1000 genomes] |
| rs73749165 | 1.00[AFR][1000 genomes] |
| rs73749166 | 1.00[AFR][1000 genomes] |
| rs73749167 | 1.00[AFR][1000 genomes] |
| rs73749168 | 1.00[AFR][1000 genomes] |
| rs73749186 | 0.87[AFR][1000 genomes] |
| rs73749188 | 0.87[AFR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:3 , 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 | nsv970339 | chr6:82201643-82207387 | Enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
