Variant report
Variant | rs12315352 |
---|---|
Chromosome Location | chr12:30008729-30008730 |
allele | A/C |
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:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr12:30007730..30010615-chr3:183415263..183417934,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000163872 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10843526 | 1.00[AFR][1000 genomes] |
rs11050472 | 0.85[AFR][1000 genomes] |
rs11050473 | 0.89[AFR][1000 genomes] |
rs11050474 | 0.89[AFR][1000 genomes] |
rs11050475 | 0.89[AFR][1000 genomes] |
rs11050476 | 0.89[AFR][1000 genomes] |
rs11050477 | 0.89[AFR][1000 genomes] |
rs11050478 | 0.89[AFR][1000 genomes] |
rs11050480 | 0.89[AFR][1000 genomes] |
rs11050481 | 0.89[AFR][1000 genomes] |
rs11050484 | 0.89[AFR][1000 genomes] |
rs11050485 | 0.89[AFR][1000 genomes] |
rs11050486 | 0.89[AFR][1000 genomes] |
rs11050487 | 0.89[AFR][1000 genomes] |
rs11050488 | 0.84[AFR][1000 genomes] |
rs11050489 | 0.84[AFR][1000 genomes] |
rs11050491 | 0.89[AFR][1000 genomes] |
rs11050492 | 0.89[AFR][1000 genomes] |
rs11050493 | 0.89[AFR][1000 genomes] |
rs11050494 | 0.89[AFR][1000 genomes] |
rs11050498 | 1.00[AFR][1000 genomes] |
rs11050499 | 1.00[AFR][1000 genomes] |
rs11050500 | 1.00[AFR][1000 genomes] |
rs11050501 | 1.00[AFR][1000 genomes] |
rs11050502 | 1.00[AFR][1000 genomes] |
rs11050503 | 1.00[AFR][1000 genomes] |
rs11050504 | 1.00[AFR][1000 genomes] |
rs11050505 | 1.00[AFR][1000 genomes] |
rs11050507 | 0.90[AFR][1000 genomes] |
rs12298049 | 0.89[AFR][1000 genomes] |
rs12300211 | 0.89[AFR][1000 genomes] |
rs12301279 | 1.00[AFR][1000 genomes] |
rs12304166 | 0.89[AFR][1000 genomes] |
rs12304207 | 0.89[AFR][1000 genomes] |
rs12304335 | 0.89[AFR][1000 genomes] |
rs12306775 | 1.00[AFR][1000 genomes] |
rs12307862 | 0.89[AFR][1000 genomes] |
rs12313116 | 1.00[AFR][1000 genomes] |
rs12314833 | 0.90[AFR][1000 genomes] |
rs12315210 | 1.00[AFR][1000 genomes] |
rs12315716 | 0.89[AFR][1000 genomes] |
rs12317098 | 0.89[AFR][1000 genomes] |
rs12317199 | 0.89[AFR][1000 genomes] |
rs12317899 | 0.89[AFR][1000 genomes] |
rs12318071 | 0.89[AFR][1000 genomes] |
rs12318077 | 0.89[AFR][1000 genomes] |
rs12320006 | 0.89[AFR][1000 genomes] |
rs12320007 | 0.89[AFR][1000 genomes] |
rs12321517 | 0.89[AFR][1000 genomes] |
rs12321611 | 0.89[AFR][1000 genomes] |
rs13313229 | 0.89[AFR][1000 genomes] |
rs13313230 | 0.89[AFR][1000 genomes] |
rs13313236 | 0.89[AFR][1000 genomes] |
rs1438510 | 0.89[AFR][1000 genomes] |
rs1438511 | 0.89[AFR][1000 genomes] |
rs1599733 | 1.00[AFR][1000 genomes] |
rs2101263 | 0.90[AFR][1000 genomes] |
rs73071616 | 0.82[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv529328 | chr12:29692414-30246209 | Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | nsv469191 | chr12:29939628-30098770 | Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
3 | nsv557958 | chr12:29939628-30098770 | ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
4 | nsv526146 | chr12:29989292-30112823 | Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
5 | nsv557975 | chr12:30000388-30022105 | Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:30008400-30014400 | Enhancers | Breast Myoepithelial Primary Cells | Breast |