Variant report
| Variant | rs11265512 |
|---|---|
| Chromosome Location | chr1:160870841-160870842 |
| allele | A/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:
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| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr1:160869759..160871916-chr1:160873094..160874895,2 | K562 | blood: |
| No data |
| No data |
| No data |
| No data |
rSNPs within LD-proxies of this variant (count:23)
| rs_ID | r2[population] |
|---|---|
| rs11265507 | 1.00[CHB][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs11265508 | 1.00[CHB][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs11265509 | 1.00[CHB][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs11265515 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs11265518 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs12049314 | 1.00[CHB][hapmap] |
| rs12058717 | 1.00[EUR][1000 genomes] |
| rs12059800 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs12060340 | 1.00[CHB][hapmap] |
| rs12064282 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs12089284 | 1.00[EUR][1000 genomes] |
| rs12095453 | 1.00[CHB][hapmap];1.00[YRI][hapmap] |
| rs13376023 | 0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs16832505 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs16832515 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs2271966 | 1.00[EUR][1000 genomes] |
| rs2295617 | 1.00[CHB][hapmap] |
| rs28541440 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs28794254 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs4129197 | 0.80[AFR][1000 genomes] |
| rs72710795 | 0.80[AFR][1000 genomes] |
| rs7553511 | 1.00[EUR][1000 genomes] |
| rs7553826 | 1.00[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:4 , 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 | nsv530077 | chr1:160836448-161284904 | Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 119 gene(s) | inside rSNPs | diseases |
| 2 | esv3430322 | chr1:160851829-160920480 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
| 3 | nsv947200 | chr1:160870136-160905390 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
| 4 | esv3347128 | chr1:160870639-160871628 | Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:160870200-160875600 | Weak transcription | Spleen | Spleen |
