Variant report
| Variant | rs73266583 |
|---|---|
| Chromosome Location | chr10:44206676-44206677 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
| No data |
| No data |
| No data |
| No data |
| No data |
rSNPs within LD-proxies of this variant (count:31)
| rs_ID | r2[population] |
|---|---|
| rs58440555 | 1.00[AFR][1000 genomes] |
| rs58605440 | 1.00[AFR][1000 genomes] |
| rs7080468 | 0.87[AFR][1000 genomes] |
| rs73265874 | 1.00[AFR][1000 genomes] |
| rs73268410 | 0.87[AFR][1000 genomes] |
| rs73268427 | 1.00[AFR][1000 genomes] |
| rs73268446 | 1.00[AFR][1000 genomes] |
| rs73268468 | 1.00[AFR][1000 genomes] |
| rs73268474 | 1.00[AFR][1000 genomes] |
| rs73268480 | 1.00[AFR][1000 genomes] |
| rs73268484 | 1.00[AFR][1000 genomes] |
| rs73270332 | 1.00[AFR][1000 genomes] |
| rs73270342 | 1.00[AFR][1000 genomes] |
| rs73270344 | 1.00[AFR][1000 genomes] |
| rs73270346 | 1.00[AFR][1000 genomes] |
| rs73270349 | 1.00[AFR][1000 genomes] |
| rs73275923 | 1.00[AFR][1000 genomes] |
| rs73275932 | 1.00[AFR][1000 genomes] |
| rs73275938 | 1.00[AFR][1000 genomes] |
| rs73275945 | 1.00[AFR][1000 genomes] |
| rs73275947 | 1.00[AFR][1000 genomes] |
| rs73275964 | 1.00[AFR][1000 genomes] |
| rs73275968 | 1.00[AFR][1000 genomes] |
| rs73275969 | 1.00[AFR][1000 genomes] |
| rs73275979 | 1.00[AFR][1000 genomes] |
| rs73276532 | 1.00[AFR][1000 genomes] |
| rs73276558 | 1.00[AFR][1000 genomes] |
| rs73276559 | 1.00[AFR][1000 genomes] |
| rs73276560 | 1.00[AFR][1000 genomes] |
| rs7904663 | 1.00[AFR][1000 genomes] |
| rs7921743 | 1.00[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 | esv3317585 | chr10:44202846-44207644 | Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
| 2 | esv3521366 | chr10:44203996-44206694 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
| 3 | esv3521368 | chr10:44203996-44206694 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr10:44203400-44207200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr10:44204200-44207000 | Weak transcription | Spleen | Spleen |
