Variant report
Variant | rs806024 |
---|---|
Chromosome Location | chr19:51403423-51403424 |
allele | C/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 | chr19:51402463..51404550-chr19:51522904..51525156,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000129451 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1090647 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1090648 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1654553 | 0.80[EUR][1000 genomes] |
rs1701941 | 0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2569530 | 0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs806020 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs806021 | 0.87[EUR][1000 genomes] |
rs806022 | 0.89[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 | nsv1060760 | chr19:50883425-51463712 | ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 99 gene(s) | inside rSNPs | diseases |
2 | nsv1058177 | chr19:50984774-51463712 | Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 84 gene(s) | inside rSNPs | diseases |
3 | nsv511623 | chr19:51400775-51408842 | Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | n/a |
No data |