Variant report
Variant | rs6714486 |
---|---|
Chromosome Location | chr2:234580305-234580306 |
allele | A/T |
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 | chr2:234578802..234581575-chr2:234598668..234600515,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000167165 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11568318 | 1.00[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap] |
rs1551286 | 0.80[EUR][1000 genomes] |
rs17862835 | 0.80[EUR][1000 genomes] |
rs17862844 | 0.80[EUR][1000 genomes] |
rs17862846 | 1.00[CEU][hapmap];0.80[EUR][1000 genomes] |
rs17862848 | 1.00[CEU][hapmap];0.80[EUR][1000 genomes] |
rs17862851 | 1.00[CEU][hapmap];0.90[EUR][1000 genomes] |
rs17862854 | 0.90[EUR][1000 genomes] |
rs17862859 | 0.88[CEU][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.95[EUR][1000 genomes] |
rs17863784 | 0.88[CEU][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.95[EUR][1000 genomes] |
rs17863795 | 1.00[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap] |
rs17864666 | 1.00[CEU][hapmap];0.80[EUR][1000 genomes] |
rs17864670 | 0.89[CEU][hapmap];0.80[EUR][1000 genomes] |
rs17864671 | 0.80[EUR][1000 genomes] |
rs17864675 | 1.00[CEU][hapmap];1.00[GIH][hapmap];0.88[TSI][hapmap];0.80[EUR][1000 genomes] |
rs17864689 | 1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.95[EUR][1000 genomes] |
rs17864691 | 0.95[EUR][1000 genomes] |
rs17864692 | 1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.95[EUR][1000 genomes] |
rs17868298 | 1.00[CEU][hapmap];0.80[EUR][1000 genomes] |
rs17868299 | 0.80[EUR][1000 genomes] |
rs17868301 | 0.80[EUR][1000 genomes] |
rs17868318 | 1.00[CEU][hapmap];0.90[EUR][1000 genomes] |
rs17868320 | 0.95[EUR][1000 genomes] |
rs17868338 | 1.00[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap] |
rs17868341 | 1.00[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap] |
rs28898590 | 0.95[EUR][1000 genomes] |
rs45507691 | 0.90[EUR][1000 genomes] |
rs56125405 | 0.92[EUR][1000 genomes] |
rs56143032 | 0.95[EUR][1000 genomes] |
rs6755571 | 0.95[EUR][1000 genomes] |
rs7563478 | 1.00[CEU][hapmap];0.80[EUR][1000 genomes] |
rs7585521 | 1.00[CEU][hapmap];1.00[GIH][hapmap];0.88[TSI][hapmap];0.90[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv529419 | chr2:234229606-234670426 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 39 gene(s) | inside rSNPs | diseases |
2 | nsv428072 | chr2:234393609-234624769 | Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
3 | nsv1010936 | chr2:234549011-234640221 | Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 21 gene(s) | inside rSNPs | diseases |
4 | nsv1013712 | chr2:234558457-235495825 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 41 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:234554600-234587800 | Weak transcription | Rectal Mucosa Donor 31 | rectum |
2 | chr2:234559800-234592800 | Weak transcription | Rectal Mucosa Donor 29 | rectum |
3 | chr2:234579800-234580600 | Flanking Active TSS | Liver | Liver |
4 | chr2:234579800-234580600 | Enhancers | A549 | lung |