Variant report
Variant | rs28438882 |
---|---|
Chromosome Location | chr14:65847859-65847860 |
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:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr14:65846264..65850153-chr14:65876897..65880691,3 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000033170 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10047886 | 0.89[AFR][1000 genomes] |
rs10130270 | 0.85[AFR][1000 genomes] |
rs10131095 | 1.00[AFR][1000 genomes] |
rs10132304 | 0.89[AFR][1000 genomes] |
rs10135430 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10135555 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10136600 | 1.00[AFR][1000 genomes] |
rs10137309 | 1.00[AMR][1000 genomes] |
rs10137961 | 1.00[AFR][1000 genomes] |
rs10138521 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10142126 | 1.00[AFR][1000 genomes] |
rs10142520 | 1.00[AFR][1000 genomes] |
rs10143378 | 1.00[AFR][1000 genomes] |
rs10143537 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10148449 | 1.00[AFR][1000 genomes] |
rs10149224 | 1.00[AFR][1000 genomes] |
rs10150033 | 1.00[AFR][1000 genomes] |
rs10150248 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10150722 | 1.00[AFR][1000 genomes] |
rs10151906 | 1.00[AFR][1000 genomes] |
rs17102622 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs1871746 | 0.89[AFR][1000 genomes] |
rs2152376 | 1.00[AFR][1000 genomes] |
rs28459646 | 0.89[AFR][1000 genomes] |
rs28462250 | 0.89[AFR][1000 genomes] |
rs28482071 | 1.00[AFR][1000 genomes] |
rs28489429 | 1.00[AFR][1000 genomes] |
rs28546829 | 0.89[AFR][1000 genomes] |
rs28550810 | 0.89[AFR][1000 genomes] |
rs28583895 | 1.00[AFR][1000 genomes] |
rs28654875 | 0.89[AFR][1000 genomes] |
rs28708772 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs9323458 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv832818 | chr14:65706859-65882320 | Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 20 gene(s) | inside rSNPs | diseases |
2 | nsv1036403 | chr14:65724229-66208114 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 35 gene(s) | inside rSNPs | diseases |
3 | nsv1043943 | chr14:65782466-66698411 | Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 55 gene(s) | inside rSNPs | diseases |
4 | nsv542120 | chr14:65782466-66698411 | Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 55 gene(s) | inside rSNPs | diseases |
5 | nsv1039168 | chr14:65811750-66308343 | Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 35 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:65840400-65850800 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
2 | chr14:65841400-65848600 | Weak transcription | Brain Substantia Nigra | brain |