Variant report
Variant | rs72696893 |
---|---|
Chromosome Location | chr4:171692146-171692147 |
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] |
---|---|
rs72698830 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72698837 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72698861 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72698875 | 0.86[EUR][1000 genomes] |
rs72698878 | 0.86[EUR][1000 genomes] |
rs72698881 | 0.86[EUR][1000 genomes] |
rs72700821 | 0.86[EUR][1000 genomes] |
rs72700825 | 0.86[EUR][1000 genomes] |
rs72700830 | 0.86[EUR][1000 genomes] |
rs72700833 | 0.86[EUR][1000 genomes] |
rs72700834 | 0.86[EUR][1000 genomes] |
rs72700840 | 0.86[EUR][1000 genomes] |
rs72700847 | 0.86[EUR][1000 genomes] |
rs72700850 | 0.86[EUR][1000 genomes] |
rs72702533 | 0.86[EUR][1000 genomes] |
rs72702562 | 0.86[EUR][1000 genomes] |
rs72981846 | 1.00[ASN][1000 genomes] |
rs72981848 | 1.00[ASN][1000 genomes] |
rs72981882 | 1.00[ASN][1000 genomes] |
rs72981885 | 1.00[ASN][1000 genomes] |
rs73868352 | 1.00[ASN][1000 genomes] |
rs7693814 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv881606 | chr4:171640683-171760509 | Active TSS Enhancers Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
2 | nsv881345 | chr4:171673765-172228547 | Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 17 gene(s) | inside rSNPs | diseases |
3 | esv275125 | chr4:171687307-171693080 | Enhancers Weak transcription | n/a | n/a | inside rSNPs | n/a |
4 | esv3508498 | chr4:171690271-171722702 | Enhancers Active TSS Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | esv3508499 | chr4:171690271-171722702 | Active TSS Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:171691400-171692800 | Weak transcription | Placenta Amnion | Placenta Amnion |