Variant report
Variant | rs13272568 |
---|---|
Chromosome Location | chr8:79034459-79034460 |
allele | A/C |
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] |
---|---|
rs10095221 | 0.85[AFR][1000 genomes] |
rs10095647 | 0.83[EUR][1000 genomes] |
rs10099895 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs10106856 | 0.82[EUR][1000 genomes] |
rs11782332 | 0.82[AMR][1000 genomes] |
rs11784050 | 1.00[ASN][1000 genomes] |
rs13258690 | 1.00[ASN][1000 genomes] |
rs13258830 | 0.88[AFR][1000 genomes] |
rs13274461 | 1.00[ASN][1000 genomes] |
rs13278866 | 0.97[ASN][1000 genomes] |
rs13281068 | 1.00[ASN][1000 genomes] |
rs1481513 | 0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs17483138 | 1.00[ASN][1000 genomes] |
rs2368503 | 1.00[ASN][1000 genomes] |
rs4308718 | 0.97[ASN][1000 genomes] |
rs62510275 | 1.00[ASN][1000 genomes] |
rs6473090 | 0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6988252 | 0.83[EUR][1000 genomes] |
rs6989455 | 0.82[EUR][1000 genomes] |
rs6991500 | 1.00[ASN][1000 genomes] |
rs7814012 | 0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs957280 | 0.91[AFR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv526123 | chr8:79008608-79046492 | Enhancers Flanking Active TSS Active TSS Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
2 | nsv525612 | chr8:79008608-79046695 | Enhancers Flanking Active TSS Weak transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
Disease | PMID | Source |
---|---|---|
Bone mineral density | 22504420 | GWAS catalog |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:79031000-79037000 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |