Variant report
Variant | rs11857698 |
---|---|
Chromosome Location | chr15:35448802-35448803 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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(count:3 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs10152519 | 0.88[EUR][1000 genomes] |
rs10152995 | 0.89[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10444813 | 0.87[EUR][1000 genomes] |
rs11073085 | 0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[ASN][1000 genomes] |
rs11073086 | 0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11854262 | 0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11854457 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11855339 | 0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1458885 | 0.88[EUR][1000 genomes] |
rs16960534 | 0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs16960587 | 0.88[EUR][1000 genomes] |
rs1903077 | 0.82[ASN][1000 genomes] |
rs2168959 | 0.92[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs4923911 | 0.99[ASN][1000 genomes] |
rs4923912 | 0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[ASN][1000 genomes] |
rs55662900 | 0.88[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs56225597 | 0.89[EUR][1000 genomes] |
rs62006770 | 0.89[EUR][1000 genomes] |
rs62006771 | 0.88[EUR][1000 genomes] |
rs6495758 | 0.88[EUR][1000 genomes] |
rs67156387 | 0.81[EUR][1000 genomes] |
rs73389201 | 0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs967370 | 0.88[EUR][1000 genomes] |
rs9944276 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3350109 | chr15:34668106-35534229 | Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 64 gene(s) | inside rSNPs | diseases |
2 | nsv522411 | chr15:34953986-35462981 | Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 43 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:35431200-35451800 | Weak transcription | Aorta | Aorta |