Variant report
| Variant | rs7560369 |
|---|---|
| Chromosome Location | chr2:12171154-12171155 |
| allele | A/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 |
rSNPs within LD-proxies of this variant (count:25)
| rs_ID | r2[population] |
|---|---|
| rs10210269 | 0.82[CHB][hapmap];0.83[JPT][hapmap] |
| rs1036670 | 0.82[ASN][1000 genomes] |
| rs10929776 | 0.87[CHB][hapmap];0.83[JPT][hapmap] |
| rs10929781 | 0.84[AMR][1000 genomes];0.93[ASN][1000 genomes] |
| rs11675063 | 0.84[AMR][1000 genomes];0.93[ASN][1000 genomes] |
| rs12471493 | 0.89[ASN][1000 genomes] |
| rs12692452 | 0.89[EUR][1000 genomes] |
| rs12987412 | 0.84[AMR][1000 genomes];0.93[ASN][1000 genomes] |
| rs13002231 | 1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes] |
| rs13007105 | 0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes] |
| rs1550395 | 1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
| rs1550396 | 1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes] |
| rs1550398 | 0.87[CHB][hapmap];0.83[JPT][hapmap] |
| rs2165219 | 0.84[AMR][1000 genomes];0.93[ASN][1000 genomes] |
| rs2165220 | 0.84[AMR][1000 genomes];0.93[ASN][1000 genomes] |
| rs2380405 | 0.91[ASN][1000 genomes] |
| rs6432249 | 0.91[ASN][1000 genomes] |
| rs6432250 | 0.91[ASN][1000 genomes] |
| rs6744092 | 0.85[ASN][1000 genomes] |
| rs751578 | 0.82[ASN][1000 genomes] |
| rs751579 | 0.94[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes] |
| rs7566729 | 0.82[ASN][1000 genomes] |
| rs7584343 | 0.84[AMR][1000 genomes];0.93[ASN][1000 genomes] |
| rs7584367 | 0.84[AMR][1000 genomes];0.93[ASN][1000 genomes] |
| rs7585074 | 0.87[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv1003899 | chr2:11789374-12248081 | Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 26 gene(s) | inside rSNPs | diseases |
| 2 | nsv999704 | chr2:12153766-12243960 | Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
| 3 | nsv1005069 | chr2:12161023-12242734 | Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
| 4 | nsv1000696 | chr2:12162843-12241022 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:12167600-12171800 | Weak transcription | K562 | blood |
| 2 | chr2:12167600-12172400 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
