Variant report
| Variant | rs59601763 |
|---|---|
| Chromosome Location | chr5:98469458-98469459 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:2 , 50 per page) page:
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| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000248489 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:19)
| rs_ID | r2[population] |
|---|---|
| rs11955910 | 0.84[AFR][1000 genomes] |
| rs11959431 | 1.00[AMR][1000 genomes] |
| rs17166664 | 0.84[AFR][1000 genomes] |
| rs17166785 | 1.00[AMR][1000 genomes] |
| rs17166795 | 1.00[AMR][1000 genomes] |
| rs60989401 | 0.84[AFR][1000 genomes] |
| rs61174020 | 1.00[AMR][1000 genomes] |
| rs6596776 | 1.00[AMR][1000 genomes] |
| rs73134022 | 1.00[AMR][1000 genomes] |
| rs73137719 | 1.00[AMR][1000 genomes] |
| rs73137720 | 1.00[AMR][1000 genomes] |
| rs73144595 | 1.00[AMR][1000 genomes] |
| rs73148439 | 0.86[AFR][1000 genomes] |
| rs73157630 | 1.00[AMR][1000 genomes] |
| rs73157639 | 1.00[AMR][1000 genomes] |
| rs73157648 | 1.00[AMR][1000 genomes] |
| rs73776747 | 1.00[AMR][1000 genomes] |
| rs73776749 | 1.00[AMR][1000 genomes] |
| rs7716779 | 1.00[AMR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page:
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| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv1024391 | chr5:98355665-98653657 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | Chromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
| 2 | nsv599118 | chr5:98358191-99029453 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
| 3 | nsv599119 | chr5:98358191-99315677 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
| 4 | nsv882417 | chr5:98428184-98548315 | Weak transcription Enhancers Flanking Active TSS | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
| 5 | nsv482367 | chr5:98440337-98606909 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
| 6 | nsv882418 | chr5:98447682-98694849 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
