Variant report
Variant | rs11948942 |
---|---|
Chromosome Location | chr5:120717195-120717196 |
allele | A/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] |
---|---|
rs11741644 | 0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11952441 | 1.00[ASN][1000 genomes] |
rs17147662 | 0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17147688 | 1.00[ASN][1000 genomes] |
rs17147694 | 1.00[ASN][1000 genomes] |
rs17147703 | 1.00[ASN][1000 genomes] |
rs17449200 | 1.00[ASN][1000 genomes] |
rs34429875 | 0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35631466 | 0.94[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs4385235 | 0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4895173 | 1.00[ASN][1000 genomes] |
rs607107 | 1.00[ASN][1000 genomes] |
rs621433 | 1.00[ASN][1000 genomes] |
rs62380463 | 0.94[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs62380506 | 1.00[ASN][1000 genomes] |
rs649659 | 1.00[ASN][1000 genomes] |
rs6595289 | 1.00[ASN][1000 genomes] |
rs6595290 | 1.00[ASN][1000 genomes] |
rs6595291 | 1.00[ASN][1000 genomes] |
rs7704634 | 0.83[AMR][1000 genomes];0.88[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv599606 | chr5:120219340-120776767 | Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv882797 | chr5:120359319-120757262 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | esv33642 | chr5:120380525-120848760 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | esv2754268 | chr5:120398198-120745053 | Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv1033162 | chr5:120685951-120736122 | Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
6 | nsv1023679 | chr5:120689805-120890257 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:120715000-120720400 | Weak transcription | Dnd41 | blood |