Variant report
Variant | rs16996587 |
---|---|
Chromosome Location | chr20:15786480-15786481 |
allele | C/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 | chr20:15784951..15787296-chr20:15795585..15797238,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs12624706 | 0.88[CEU][hapmap];1.00[GIH][hapmap];0.85[MEX][hapmap];0.96[TSI][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs13039564 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs13041254 | 0.88[CEU][hapmap] |
rs13042688 | 0.94[CEU][hapmap];0.82[CHB][hapmap];0.95[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs13044785 | 0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs1997798 | 0.91[EUR][1000 genomes] |
rs2109535 | 0.85[EUR][1000 genomes] |
rs2109536 | 0.91[EUR][1000 genomes] |
rs2327966 | 0.93[CEU][hapmap] |
rs35973686 | 0.86[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs36034970 | 0.94[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs4292145 | 0.88[EUR][1000 genomes] |
rs4426588 | 0.88[EUR][1000 genomes] |
rs4627651 | 0.94[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs4813196 | 0.85[TSI][hapmap] |
rs6034288 | 0.83[CEU][hapmap] |
rs6043529 | 0.81[CEU][hapmap] |
rs6043530 | 0.81[CEU][hapmap] |
rs6043539 | 0.88[CEU][hapmap] |
rs6131701 | 0.82[CEU][hapmap] |
rs6131706 | 0.84[EUR][1000 genomes] |
rs6131713 | 0.92[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs6131714 | 0.88[CEU][hapmap];0.91[EUR][1000 genomes] |
rs6131715 | 0.88[CEU][hapmap];0.91[EUR][1000 genomes] |
rs6131716 | 0.88[CEU][hapmap];0.91[EUR][1000 genomes] |
rs6131717 | 0.88[CEU][hapmap];0.91[EUR][1000 genomes] |
rs6131718 | 0.88[CEU][hapmap];0.90[EUR][1000 genomes] |
rs6131727 | 0.94[CEU][hapmap];0.82[CHB][hapmap];0.81[YRI][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs6135506 | 0.88[CEU][hapmap] |
rs6135508 | 0.88[CEU][hapmap] |
rs6135509 | 0.88[CEU][hapmap];0.81[GIH][hapmap];0.84[TSI][hapmap] |
rs6135511 | 1.00[CEU][hapmap];0.83[EUR][1000 genomes] |
rs6135512 | 0.88[CEU][hapmap] |
rs6135514 | 0.88[CEU][hapmap] |
rs6135519 | 0.84[EUR][1000 genomes] |
rs6135520 | 0.88[CEU][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs6135521 | 0.84[GIH][hapmap];0.88[TSI][hapmap];0.84[EUR][1000 genomes] |
rs6135528 | 0.94[CEU][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs6135529 | 0.94[CEU][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs6135530 | 0.94[CEU][hapmap];0.87[GIH][hapmap];0.84[MEX][hapmap];0.92[TSI][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs6135531 | 0.93[CEU][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs6135543 | 0.94[CEU][hapmap];0.82[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6135545 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6135557 | 0.89[CHD][hapmap];0.93[GIH][hapmap];0.81[LWK][hapmap];0.91[YRI][hapmap] |
rs62194716 | 0.80[AMR][1000 genomes] |
rs6514613 | 0.93[CEU][hapmap] |
rs7269144 | 1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs7273944 | 1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs761262 | 0.88[CEU][hapmap];0.93[TSI][hapmap];0.91[EUR][1000 genomes] |
rs764140 | 0.88[CEU][hapmap];0.81[GIH][hapmap];0.84[TSI][hapmap] |
rs877270 | 1.00[CEU][hapmap] |
rs877271 | 1.00[CEU][hapmap] |
rs979530 | 0.91[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869328 | chr20:15325423-16213898 | Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv519883 | chr20:15738086-15817106 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv585643 | chr20:15759361-15796051 | Flanking Active TSS Enhancers Weak transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv912793 | chr20:15760969-15807441 | Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | nsv833929 | chr20:15765372-15977337 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
6 | esv1847965 | chr20:15766727-15807441 | Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | nsv585644 | chr20:15766727-15807441 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
8 | esv2754713 | chr20:15785800-15816800 | Enhancers Weak transcription Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr20:15785600-15787200 | Enhancers | Brain Hippocampus Middle | brain |
2 | chr20:15786400-15790400 | Enhancers | Primary B cells from peripheral blood | blood |