Variant report
Variant | rs13435562 |
---|---|
Chromosome Location | chr4:47111548-47111549 |
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] |
---|---|
rs10011073 | 0.89[YRI][hapmap] |
rs10011533 | 0.89[YRI][hapmap] |
rs10014305 | 1.00[AFR][1000 genomes] |
rs10016131 | 1.00[YRI][hapmap];1.00[AFR][1000 genomes] |
rs10023824 | 0.90[YRI][hapmap] |
rs10023997 | 1.00[YRI][hapmap] |
rs10027905 | 1.00[YRI][hapmap];1.00[AFR][1000 genomes] |
rs28385901 | 1.00[AFR][1000 genomes] |
rs28428700 | 1.00[AFR][1000 genomes] |
rs28479557 | 1.00[AFR][1000 genomes] |
rs28564010 | 0.80[AFR][1000 genomes] |
rs28722026 | 1.00[AFR][1000 genomes] |
rs6818487 | 1.00[YRI][hapmap] |
rs9291302 | 1.00[YRI][hapmap];1.00[AFR][1000 genomes] |
rs9997149 | 1.00[AFR][1000 genomes] |
rs9997150 | 1.00[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv537078 | chr4:47059778-47137372 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
2 | nsv829922 | chr4:47093785-47261181 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
3 | nsv879003 | chr4:47102993-47215939 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
No data |