Variant report
Variant | rs9301781 |
---|---|
Chromosome Location | chr13:92828151-92828152 |
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 | chr13:92598450..92599301-chr13:92827714..92828302,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10492504 | 1.00[CHB][hapmap] |
rs1172297 | 1.00[CHB][hapmap] |
rs1177726 | 1.00[CHB][hapmap] |
rs1330978 | 1.00[CHB][hapmap] |
rs1330982 | 1.00[CHB][hapmap] |
rs1330983 | 1.00[CHB][hapmap] |
rs1330984 | 1.00[CHB][hapmap] |
rs1330995 | 1.00[CHB][hapmap] |
rs1411747 | 1.00[CHB][hapmap] |
rs16947132 | 1.00[CHB][hapmap] |
rs16947150 | 1.00[CHB][hapmap] |
rs17267151 | 1.00[CHB][hapmap] |
rs17426071 | 1.00[CHB][hapmap] |
rs2148521 | 1.00[CHB][hapmap] |
rs2182533 | 1.00[CHB][hapmap] |
rs2209651 | 1.00[CHB][hapmap] |
rs4408406 | 1.00[CHB][hapmap] |
rs4771854 | 1.00[CHB][hapmap] |
rs6650316 | 1.00[CHB][hapmap] |
rs7334533 | 1.00[CHB][hapmap] |
rs7336644 | 1.00[CHB][hapmap] |
rs7489550 | 1.00[CHB][hapmap] |
rs7987741 | 1.00[CHB][hapmap] |
rs7991537 | 1.00[CHB][hapmap] |
rs880546 | 1.00[CHB][hapmap] |
rs9301782 | 1.00[CHB][hapmap];1.00[AMR][1000 genomes] |
rs9523526 | 1.00[CHB][hapmap] |
rs9523535 | 1.00[CHB][hapmap] |
rs9556163 | 1.00[CHB][hapmap] |
rs9560982 | 1.00[CHB][hapmap] |
rs9560983 | 1.00[CHB][hapmap] |
rs9560984 | 1.00[CHB][hapmap] |
rs9560986 | 1.00[CHB][hapmap] |
rs9560988 | 1.00[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2756005 | chr13:92584199-93080799 | Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv456066 | chr13:92694581-92884370 | Enhancers Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
3 | nsv562723 | chr13:92694581-92884370 | Flanking Active TSS Active TSS Enhancers Weak transcription | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
4 | nsv1035365 | chr13:92805325-92926114 | Enhancers Weak transcription Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
5 | nsv1053468 | chr13:92814581-92893231 | Enhancers Active TSS Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:92827600-92828200 | Active TSS | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |