Variant report
Variant | rs9324802 |
---|---|
Chromosome Location | chr5:154459454-154459455 |
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] |
---|---|
rs10038694 | 0.85[EUR][1000 genomes] |
rs10038971 | 0.82[EUR][1000 genomes] |
rs10223164 | 0.87[EUR][1000 genomes] |
rs11167708 | 0.94[CEU][hapmap];0.87[EUR][1000 genomes] |
rs11167709 | 0.87[EUR][1000 genomes] |
rs11167711 | 0.81[EUR][1000 genomes] |
rs12153386 | 0.94[CEU][hapmap];0.87[EUR][1000 genomes] |
rs12187210 | 0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs12188764 | 0.87[EUR][1000 genomes] |
rs12188773 | 0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs12519670 | 0.94[CEU][hapmap];0.87[EUR][1000 genomes] |
rs34021636 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34121599 | 0.87[EUR][1000 genomes] |
rs35235180 | 0.87[EUR][1000 genomes] |
rs4958396 | 0.87[EUR][1000 genomes] |
rs4958776 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs4958780 | 0.87[EUR][1000 genomes] |
rs6868742 | 0.94[CEU][hapmap];0.87[EUR][1000 genomes] |
rs6868904 | 0.94[CEU][hapmap];0.87[EUR][1000 genomes] |
rs6890088 | 0.87[EUR][1000 genomes] |
rs6890098 | 0.94[CEU][hapmap];0.87[EUR][1000 genomes] |
rs6890664 | 0.86[EUR][1000 genomes] |
rs6898774 | 0.94[CEU][hapmap];0.87[EUR][1000 genomes] |
rs9285651 | 0.87[EUR][1000 genomes] |
rs9324803 | 0.83[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs988435 | 0.87[EUR][1000 genomes] |
rs991314 | 0.87[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1023588 | chr5:154415586-154464455 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS | Chromatin interactive region | 2 gene(s) | inside rSNPs | n/a |
2 | nsv883059 | chr5:154457905-154556230 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:154457000-154459800 | Weak transcription | Fetal Heart | heart |