Variant report
Variant | rs7821160 |
---|---|
Chromosome Location | chr8:57986281-57986282 |
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 | chr8:57983788..57988460-chr8:57989645..57992930,4 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10958519 | 0.83[CHD][hapmap] |
rs10958522 | 0.81[JPT][hapmap] |
rs10958523 | 0.86[JPT][hapmap] |
rs11776524 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11777459 | 0.85[CHB][hapmap];0.91[JPT][hapmap] |
rs12216730 | 0.88[ASN][1000 genomes] |
rs1596142 | 0.85[CHB][hapmap];0.91[JPT][hapmap] |
rs16921623 | 0.89[CHB][hapmap];0.89[JPT][hapmap] |
rs16921626 | 0.85[CHB][hapmap];0.90[JPT][hapmap] |
rs16921675 | 0.89[CHB][hapmap];0.90[JPT][hapmap] |
rs16921676 | 0.80[CHB][hapmap];0.91[JPT][hapmap] |
rs2218271 | 0.85[CHB][hapmap];0.91[JPT][hapmap] |
rs4541915 | 0.83[ASN][1000 genomes] |
rs4590436 | 0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4738567 | 0.88[ASN][1000 genomes] |
rs4738578 | 0.81[CHB][hapmap];0.91[JPT][hapmap] |
rs55923836 | 0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs58244172 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs59072740 | 0.87[AFR][1000 genomes];0.88[EUR][1000 genomes] |
rs59424848 | 0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6474098 | 0.83[ASN][1000 genomes] |
rs7000752 | 0.85[CHB][hapmap];0.91[JPT][hapmap] |
rs7814707 | 0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs9771646 | 0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs9772760 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1029443 | chr8:57748114-58057656 | Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
2 | esv3430321 | chr8:57858417-58055129 | Strong transcription Genic enhancers Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 5 gene(s) | inside rSNPs | diseases |
3 | nsv1027125 | chr8:57891279-58095884 | Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | esv2758161 | chr8:57930392-58474449 | Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
5 | esv2759618 | chr8:57930392-58474449 | Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
6 | nsv508510 | chr8:57967028-57994116 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:57981600-57988600 | Weak transcription | Pancreas | Pancrea |