Variant report
Variant | rs11586557 |
---|---|
Chromosome Location | chr1:159765165-159765166 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
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Variant related genes | Relation type |
---|---|
ENSG00000266458 | Chromatin interaction |
ENSG00000213085 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11584071 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs11585055 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs11585210 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs11585323 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs11586456 | 1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes] |
rs11586788 | 1.00[CEU][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs11587247 | 1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes] |
rs12077947 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2494495 | 1.00[JPT][hapmap] |
rs2501343 | 1.00[JPT][hapmap] |
rs2501344 | 1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes] |
rs60602471 | 0.89[AFR][1000 genomes] |
rs74124721 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1005195 | chr1:159452759-159910337 | Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 90 gene(s) | inside rSNPs | diseases |
2 | nsv521503 | chr1:159762120-159795478 | Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:159765000-159765400 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |