Variant report
Variant | rs11856282 |
---|---|
Chromosome Location | chr15:53518158-53518159 |
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 | chr15:53516800..53518385-chr15:53519039..53521500,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10163134 | 0.81[AFR][1000 genomes] |
rs10851535 | 0.88[AFR][1000 genomes] |
rs11632242 | 0.87[AFR][1000 genomes] |
rs11632644 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11633541 | 0.81[AFR][1000 genomes] |
rs11857258 | 0.87[AFR][1000 genomes] |
rs12593169 | 0.88[AFR][1000 genomes] |
rs12901316 | 0.88[AFR][1000 genomes] |
rs12908835 | 0.87[AFR][1000 genomes] |
rs1356861 | 0.88[AFR][1000 genomes] |
rs1911687 | 0.87[AFR][1000 genomes] |
rs2661577 | 0.87[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4545759 | 0.81[AFR][1000 genomes] |
rs4551981 | 0.81[AFR][1000 genomes] |
rs4577024 | 0.81[AFR][1000 genomes] |
rs6493617 | 0.88[AFR][1000 genomes] |
rs7167895 | 0.88[AFR][1000 genomes] |
rs7170453 | 0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7171938 | 0.88[AFR][1000 genomes] |
rs7172105 | 0.88[AFR][1000 genomes] |
rs8027357 | 0.87[AFR][1000 genomes] |
rs8027387 | 0.87[AFR][1000 genomes] |
rs8027674 | 0.87[AFR][1000 genomes] |
rs8042542 | 0.88[AFR][1000 genomes] |
rs8043044 | 0.87[AFR][1000 genomes] |
rs931916 | 0.86[AFR][1000 genomes] |
rs931917 | 0.81[AFR][1000 genomes] |
rs931918 | 0.87[AFR][1000 genomes] |
rs931919 | 0.87[AFR][1000 genomes] |
rs9920052 | 0.84[AFR][1000 genomes] |
rs9920819 | 0.83[AMR][1000 genomes];0.88[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3343986 | chr15:53284440-53571936 | Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv1037630 | chr15:53324645-53708925 | Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
3 | nsv1051634 | chr15:53459129-53565627 | Enhancers Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv3385784 | chr15:53492461-53521900 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:53512200-53519800 | Weak transcription | HepG2 | liver |
2 | chr15:53518000-53519800 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |