Variant report
Variant | rs6878470 |
---|---|
Chromosome Location | chr5:41541003-41541004 |
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 |
rs_ID | r2[population] |
---|---|
rs57298536 | 0.92[AFR][1000 genomes] |
rs57590605 | 0.92[AFR][1000 genomes] |
rs59447468 | 0.92[AFR][1000 genomes] |
rs59814375 | 0.92[AFR][1000 genomes] |
rs60682637 | 0.92[AFR][1000 genomes] |
rs60707515 | 0.92[AFR][1000 genomes] |
rs6877857 | 0.92[AFR][1000 genomes] |
rs6878319 | 1.00[AFR][1000 genomes] |
rs6896481 | 1.00[AFR][1000 genomes] |
rs6896632 | 1.00[AFR][1000 genomes] |
rs73081539 | 0.89[AFR][1000 genomes] |
rs73081544 | 0.92[AFR][1000 genomes] |
rs73081547 | 0.86[AFR][1000 genomes] |
rs73081549 | 0.92[AFR][1000 genomes] |
rs73081560 | 0.92[AFR][1000 genomes] |
rs73081564 | 0.92[AFR][1000 genomes] |
rs73081567 | 0.92[AFR][1000 genomes] |
rs73081569 | 0.92[AFR][1000 genomes] |
rs73081571 | 0.92[AFR][1000 genomes] |
rs73081574 | 0.92[AFR][1000 genomes] |
rs73081580 | 0.92[AFR][1000 genomes] |
rs73081589 | 0.92[AFR][1000 genomes] |
rs73081590 | 0.92[AFR][1000 genomes] |
rs73081593 | 0.92[AFR][1000 genomes] |
rs73081595 | 0.92[AFR][1000 genomes] |
rs73081599 | 0.92[AFR][1000 genomes] |
rs73083608 | 1.00[AFR][1000 genomes] |
rs73083611 | 1.00[AFR][1000 genomes] |
rs7705479 | 0.92[AFR][1000 genomes] |
rs7709197 | 1.00[MKK][hapmap] |
rs7730181 | 0.92[AFR][1000 genomes] |
rs7730189 | 1.00[YRI][hapmap];0.92[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1028390 | chr5:41537220-41561373 | Weak transcription Enhancers Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:41540200-41541200 | Weak transcription | Fetal Heart | heart |