Variant report
Variant | rs1495889 |
---|---|
Chromosome Location | chr3:86411527-86411528 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
(count:1 , 50 per page) page:
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-CADM2-9 | chr3:86411282-86411624 | NONHSAT090671 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10470569 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs11127937 | 0.87[EUR][1000 genomes] |
rs1170215 | 0.83[ASN][1000 genomes] |
rs12492844 | 0.80[EUR][1000 genomes] |
rs13059931 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1390422 | 0.83[ASN][1000 genomes] |
rs1603322 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs2201580 | 0.83[ASN][1000 genomes] |
rs2669408 | 0.82[ASN][1000 genomes] |
rs34391385 | 0.82[EUR][1000 genomes] |
rs35318836 | 0.87[EUR][1000 genomes] |
rs67481458 | 0.80[EUR][1000 genomes] |
rs6796293 | 0.83[EUR][1000 genomes] |
rs7623852 | 0.87[EUR][1000 genomes] |
rs9876219 | 0.80[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs9877726 | 0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv532629 | chr3:85763873-86608579 | Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
2 | nsv877115 | chr3:86278951-86554319 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
3 | nsv834753 | chr3:86386749-86546500 | Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |