Variant report
Variant | rs17464658 |
---|---|
Chromosome Location | chr7:25633538-25633539 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr7:25631774..25634150-chr7:25636240..25639148,2 | K562 | blood: |
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-NPVF-5 | chr7:25632971-25634336 | ENSG00000223561.2 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10486407 | 0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs10499566 | 0.81[CEU][hapmap];1.00[MEX][hapmap] |
rs1074503 | 0.92[ASN][1000 genomes] |
rs1074504 | 0.92[ASN][1000 genomes] |
rs10951079 | 0.92[ASN][1000 genomes] |
rs11971048 | 0.92[ASN][1000 genomes] |
rs11981833 | 0.92[ASN][1000 genomes] |
rs11981887 | 0.92[ASN][1000 genomes] |
rs11982106 | 0.92[ASN][1000 genomes] |
rs12216588 | 0.92[ASN][1000 genomes] |
rs1502949 | 0.92[ASN][1000 genomes] |
rs1502950 | 0.92[ASN][1000 genomes] |
rs1540332 | 0.92[ASN][1000 genomes] |
rs17367291 | 0.92[ASN][1000 genomes] |
rs17367619 | 0.80[AMR][1000 genomes] |
rs1995437 | 0.86[AFR][1000 genomes] |
rs2074137 | 0.92[ASN][1000 genomes] |
rs2188859 | 0.80[AMR][1000 genomes] |
rs3887045 | 0.92[ASN][1000 genomes] |
rs73693187 | 0.92[ASN][1000 genomes] |
rs739624 | 0.92[ASN][1000 genomes] |
rs882101 | 0.92[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1016813 | chr7:25405859-26150509 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 108 gene(s) | inside rSNPs | diseases |
2 | nsv538803 | chr7:25405859-26150509 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 108 gene(s) | inside rSNPs | diseases |
3 | esv2753823 | chr7:25626156-25655093 | Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | n/a |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:25631600-25634800 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |