Variant report
| Variant | rs2174252 |
|---|---|
| Chromosome Location | chr2:125418292-125418293 |
| allele | A/G |
| 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:22)
| rs_ID | r2[population] |
|---|---|
| rs10195554 | 1.00[CHB][hapmap] |
| rs11123056 | 1.00[YRI][hapmap] |
| rs11675141 | 1.00[YRI][hapmap] |
| rs11676952 | 1.00[YRI][hapmap] |
| rs11679251 | 1.00[JPT][hapmap] |
| rs12473828 | 0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs12473959 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs13033694 | 0.81[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs1394146 | 1.00[YRI][hapmap] |
| rs1587788 | 1.00[YRI][hapmap] |
| rs17011825 | 0.87[ASN][1000 genomes] |
| rs17392807 | 1.00[CHB][hapmap];0.88[JPT][hapmap] |
| rs17392884 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs2174251 | 0.96[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
| rs34027199 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs4473385 | 1.00[CHB][hapmap];0.88[JPT][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs4588196 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
| rs4848956 | 0.85[YRI][hapmap] |
| rs6737833 | 0.84[CEU][hapmap];0.88[JPT][hapmap] |
| rs768318 | 0.86[CEU][hapmap];0.87[EUR][1000 genomes] |
| rs768319 | 0.83[CEU][hapmap];0.85[YRI][hapmap];0.87[EUR][1000 genomes] |
| rs924803 | 1.00[YRI][hapmap] |
Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv834357 | chr2:125258157-125421507 | Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
| 2 | nsv834359 | chr2:125367872-125536022 | Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS | TF binding regionCpG island | 1 gene(s) | inside rSNPs | diseases |
| 3 | nsv428727 | chr2:125372897-125512949 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS | TF binding regionCpG island | 1 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
