Variant report
| Variant | rs72845026 |
|---|---|
| Chromosome Location | chr2:125399375-125399376 |
| 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 |
rSNPs within LD-proxies of this variant (count:27)
| rs_ID | r2[population] |
|---|---|
| rs1454139 | 0.88[EUR][1000 genomes] |
| rs1504016 | 1.00[EUR][1000 genomes] |
| rs17011851 | 0.88[EUR][1000 genomes] |
| rs17011859 | 0.88[EUR][1000 genomes] |
| rs17011865 | 0.88[EUR][1000 genomes] |
| rs59167655 | 1.00[AMR][1000 genomes];0.94[EUR][1000 genomes] |
| rs66820110 | 0.88[EUR][1000 genomes] |
| rs72841382 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
| rs72841384 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs72841386 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs72841388 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs72841390 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs72845015 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs72845059 | 1.00[AFR][1000 genomes];0.88[EUR][1000 genomes] |
| rs72845077 | 1.00[AFR][1000 genomes];0.88[EUR][1000 genomes] |
| rs72845078 | 1.00[AFR][1000 genomes];0.88[EUR][1000 genomes] |
| rs72845079 | 1.00[AFR][1000 genomes];0.88[EUR][1000 genomes] |
| rs72845081 | 1.00[AFR][1000 genomes];0.88[EUR][1000 genomes] |
| rs72845253 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs72845255 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs72845257 | 1.00[AMR][1000 genomes] |
| rs72845873 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
| rs72845874 | 1.00[AFR][1000 genomes];0.88[EUR][1000 genomes] |
| rs72845877 | 1.00[AFR][1000 genomes];0.88[EUR][1000 genomes] |
| rs72845878 | 1.00[AFR][1000 genomes];0.88[EUR][1000 genomes] |
| rs72845884 | 1.00[AFR][1000 genomes];0.88[EUR][1000 genomes] |
| rs72845901 | 1.00[AFR][1000 genomes] |
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 |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:125398200-125399800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr2:125398800-125399600 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
