Variant report
Variant | rs7024986 |
---|---|
Chromosome Location | chr9:101280146-101280147 |
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 | chr9:101277814..101279969-chr9:101280014..101283409,3 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10121121 | 0.94[AFR][1000 genomes] |
rs10733671 | 0.94[AFR][1000 genomes] |
rs2095121 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs2779556 | 0.93[ASN][1000 genomes] |
rs2779557 | 0.93[ASN][1000 genomes] |
rs2779563 | 1.00[ASN][1000 genomes] |
rs2779565 | 0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2779575 | 0.95[ASN][1000 genomes] |
rs2779577 | 0.95[ASN][1000 genomes] |
rs2779579 | 0.95[ASN][1000 genomes] |
rs2779580 | 0.95[ASN][1000 genomes] |
rs2779583 | 0.95[ASN][1000 genomes] |
rs2779586 | 0.95[ASN][1000 genomes] |
rs2779589 | 0.95[ASN][1000 genomes] |
rs2779590 | 0.93[ASN][1000 genomes] |
rs2779591 | 0.95[ASN][1000 genomes] |
rs2779593 | 0.95[ASN][1000 genomes] |
rs2808565 | 1.00[ASN][1000 genomes] |
rs2808567 | 1.00[ASN][1000 genomes] |
rs871797 | 0.93[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv430085 | chr9:100928245-101339645 | Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
2 | nsv831665 | chr9:101170061-101367692 | Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv614936 | chr9:101182698-101680380 | Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 21 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:101275800-101282800 | Weak transcription | Fetal Brain Male | brain |