Variant report
Variant | rs17006030 |
---|---|
Chromosome Location | chr4:120707217-120707218 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:5)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:5 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr4:120479930..120480751-chr4:120707167..120707918,2 | MCF-7 | breast: | |
2 | chr4:120548044..120548846-chr4:120706901..120707428,2 | MCF-7 | breast: | |
3 | chr4:120549764..120550693-chr4:120706700..120708032,11 | MCF-7 | breast: | |
4 | chr4:120549798..120550595-chr4:120706962..120707690,2 | MCF-7 | breast: | |
5 | chr4:120548325..120550738-chr4:120706107..120708454,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000138735 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs17006542 | 1.00[AMR][1000 genomes] |
rs72906585 | 1.00[AMR][1000 genomes] |
rs72906587 | 1.00[AMR][1000 genomes] |
rs72908405 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv916641 | chr4:119780023-120777320 | Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 72 gene(s) | inside rSNPs | diseases |
2 | nsv532739 | chr4:120392824-121098103 | Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 33 gene(s) | inside rSNPs | diseases |
No data |