Variant report
Variant | rs6110655 |
---|---|
Chromosome Location | chr20:15509110-15509111 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1233715 | 0.85[CEU][hapmap] |
rs1233727 | 0.92[CEU][hapmap] |
rs1233738 | 0.92[CEU][hapmap] |
rs1345368 | 0.85[CEU][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap] |
rs1547972 | 0.88[CHB][hapmap];0.82[JPT][hapmap] |
rs16995898 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap] |
rs16995992 | 0.86[EUR][1000 genomes] |
rs1816000 | 1.00[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];0.84[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap] |
rs2058735 | 0.97[ASN][1000 genomes] |
rs6034213 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs6043349 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs6043350 | 1.00[CHB][hapmap];0.92[CHD][hapmap];0.83[JPT][hapmap];1.00[MEX][hapmap] |
rs6043351 | 1.00[CHB][hapmap];0.92[CHD][hapmap];0.83[JPT][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap] |
rs6043354 | 0.84[CEU][hapmap] |
rs6105428 | 1.00[CHB][hapmap];0.92[CHD][hapmap];0.83[JPT][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.87[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs6105432 | 0.84[CEU][hapmap];0.86[TSI][hapmap];0.83[EUR][1000 genomes] |
rs6110664 | 0.85[CEU][hapmap] |
rs6135432 | 0.92[JPT][hapmap];0.86[ASN][1000 genomes] |
rs66767980 | 0.95[ASN][1000 genomes] |
rs73100235 | 0.83[EUR][1000 genomes] |
rs73100255 | 0.86[EUR][1000 genomes] |
rs9917445 | 0.88[CHB][hapmap];0.89[CHD][hapmap];0.83[JPT][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap] |
Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1062252 | chr20:14964258-15547739 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | nsv544206 | chr20:14964258-15547739 | Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | 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 |
4 | nsv833927 | chr20:15362602-15520185 | Enhancers Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | esv2751909 | chr20:15489871-15656007 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
6 | nsv518630 | chr20:15509110-15509729 | Enhancers | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr20:15509000-15509400 | Enhancers | Ovary | ovary |
2 | chr20:15509000-15509800 | Enhancers | Placenta | Placenta |
3 | chr20:15509000-15510000 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |