Variant report
Variant | rs6079728 |
---|---|
Chromosome Location | chr20:15265099-15265100 |
allele | G/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] |
---|---|
rs1304179 | 1.00[JPT][hapmap] |
rs1322114 | 1.00[CHB][hapmap] |
rs16995525 | 1.00[JPT][hapmap] |
rs17299383 | 1.00[JPT][hapmap] |
rs175273 | 1.00[CHB][hapmap] |
rs175284 | 1.00[CHB][hapmap] |
rs2180525 | 1.00[CHB][hapmap] |
rs6034141 | 1.00[CEU][hapmap] |
rs6034142 | 0.84[CEU][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes] |
rs6034145 | 1.00[JPT][hapmap] |
rs6034151 | 1.00[JPT][hapmap] |
rs6034152 | 1.00[JPT][hapmap] |
rs6034196 | 1.00[CHB][hapmap] |
rs6043164 | 0.84[CEU][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs6043165 | 1.00[JPT][hapmap] |
rs6043166 | 0.83[CEU][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs6043169 | 1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs6043199 | 1.00[JPT][hapmap] |
rs6043294 | 1.00[CHB][hapmap] |
rs6043298 | 1.00[CHB][hapmap] |
rs6043303 | 1.00[CHB][hapmap] |
rs6043305 | 1.00[CHB][hapmap] |
rs6043308 | 1.00[CHB][hapmap] |
rs6079727 | 0.94[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6105362 | 1.00[CHB][hapmap] |
rs6110525 | 1.00[CHB][hapmap] |
rs6110540 | 1.00[CHB][hapmap] |
rs6110617 | 1.00[CHB][hapmap] |
rs8115953 | 1.00[CHB][hapmap] |
Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1065152 | chr20:14781684-15305258 | Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
2 | 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 |
3 | 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 |
4 | nsv524481 | chr20:15007730-15382919 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
5 | nsv916795 | chr20:15041479-15345528 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
6 | nsv1060275 | chr20:15084485-15327541 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
7 | nsv1058827 | chr20:15159151-15289719 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
8 | nsv1058890 | chr20:15234769-15388360 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
9 | esv2755557 | chr20:15250014-15323282 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr20:15259400-15277600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |