Variant report
Variant | rs7578835 |
---|---|
Chromosome Location | chr2:125373757-125373758 |
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 |
rs_ID | r2[population] |
---|---|
rs10165603 | 0.84[CEU][hapmap];0.81[JPT][hapmap] |
rs10194805 | 0.85[CEU][hapmap];0.81[JPT][hapmap] |
rs10195187 | 0.84[CEU][hapmap];0.81[JPT][hapmap] |
rs11123053 | 0.85[CEU][hapmap];0.81[JPT][hapmap] |
rs11681388 | 0.81[JPT][hapmap] |
rs12466900 | 0.81[CEU][hapmap];0.81[JPT][hapmap] |
rs12618619 | 0.81[CEU][hapmap] |
rs12990799 | 0.81[JPT][hapmap] |
rs1504019 | 0.81[CEU][hapmap] |
rs1504020 | 0.81[CEU][hapmap] |
rs1910528 | 0.85[CEU][hapmap];0.81[JPT][hapmap] |
rs2047874 | 0.85[CEU][hapmap];0.81[JPT][hapmap] |
rs4364025 | 0.81[CEU][hapmap] |
rs4848940 | 0.81[CEU][hapmap] |
rs6541962 | 0.85[CEU][hapmap] |
rs6744929 | 0.81[CEU][hapmap] |
rs6757634 | 0.81[CEU][hapmap] |
rs6757796 | 0.81[CEU][hapmap] |
rs7558706 | 0.85[CEU][hapmap];0.81[JPT][hapmap];0.85[YRI][hapmap] |
rs7584599 | 0.85[CEU][hapmap];0.81[JPT][hapmap];0.88[YRI][hapmap] |
rs7591540 | 0.85[CEU][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.81[AMR][1000 genomes] |

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 | nsv528674 | chr2:125346337-125383522 | Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS | n/a | n/a | inside rSNPs | diseases |
3 | 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 |
4 | 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 | chr2:125373200-125373800 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |