Variant report
Variant | rs11908251 |
---|---|
Chromosome Location | chr20:24350665-24350666 |
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:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr20:24347069..24348854-chr20:24350597..24353212,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11905416 | 1.00[EUR][1000 genomes] |
rs11907190 | 1.00[EUR][1000 genomes] |
rs11907337 | 1.00[EUR][1000 genomes] |
rs11907441 | 1.00[EUR][1000 genomes] |
rs1475408 | 1.00[EUR][1000 genomes] |
rs1603419 | 1.00[EUR][1000 genomes] |
rs57839314 | 1.00[EUR][1000 genomes] |
rs6036734 | 1.00[EUR][1000 genomes] |
rs6036735 | 1.00[EUR][1000 genomes] |
rs6036736 | 1.00[EUR][1000 genomes] |
rs6036738 | 1.00[EUR][1000 genomes] |
rs6036739 | 1.00[EUR][1000 genomes] |
rs6036740 | 1.00[EUR][1000 genomes] |
rs60401696 | 1.00[EUR][1000 genomes] |
rs6049582 | 1.00[EUR][1000 genomes] |
rs6049583 | 1.00[EUR][1000 genomes] |
rs6049584 | 1.00[EUR][1000 genomes] |
rs6049586 | 1.00[EUR][1000 genomes] |
rs6049587 | 1.00[EUR][1000 genomes] |
rs6049588 | 1.00[EUR][1000 genomes] |
rs6049591 | 1.00[EUR][1000 genomes] |
rs6049592 | 1.00[EUR][1000 genomes] |
rs6049596 | 1.00[EUR][1000 genomes] |
rs6049597 | 1.00[EUR][1000 genomes] |
rs6049599 | 1.00[EUR][1000 genomes] |
rs6049600 | 1.00[EUR][1000 genomes] |
rs6049602 | 1.00[EUR][1000 genomes] |
rs6049605 | 1.00[EUR][1000 genomes] |
rs6114706 | 1.00[EUR][1000 genomes] |
rs7273213 | 1.00[EUR][1000 genomes] |
rs73339982 | 1.00[EUR][1000 genomes] |
rs73341652 | 1.00[EUR][1000 genomes] |
rs7346006 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv9793 | chr20:23939613-24734850 | Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
2 | nsv1058146 | chr20:24210196-24531087 | Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv833946 | chr20:24320375-24490702 | Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr20:24346000-24351600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr20:24349200-24360000 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |