Variant report
Variant | rs55935462 |
---|---|
Chromosome Location | chr9:72298318-72298319 |
allele | A/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 | chr9:72286480..72288672-chr9:72297057..72299109,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000107282 | Chromatin interaction |
ENSG00000261447 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs56282813 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs60544576 | 1.00[AMR][1000 genomes] |
rs60814527 | 1.00[AMR][1000 genomes] |
rs61068557 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73444509 | 1.00[AMR][1000 genomes] |
rs73444511 | 1.00[AMR][1000 genomes] |
rs73444521 | 1.00[AMR][1000 genomes] |
rs73444537 | 1.00[AMR][1000 genomes] |
rs73461031 | 1.00[AMR][1000 genomes] |
rs73461052 | 1.00[AMR][1000 genomes] |
rs73461069 | 1.00[AMR][1000 genomes] |
rs73461071 | 1.00[AMR][1000 genomes] |
rs73647272 | 1.00[AMR][1000 genomes] |
rs73647274 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv471309 | chr9:72273898-72410323 | Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
2 | esv3397197 | chr9:72298160-72299128 | Inactive region | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | esv3327668 | chr9:72298252-72298740 | Inactive region | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |