Variant report
Variant | rs17149 |
---|---|
Chromosome Location | chr12:83851319-83851320 |
allele | G/T |
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-CCDC59-5 | chr12:83850418-83852731 | XLOC_010142 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10746276 | 0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs10778977 | 0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10862638 | 0.86[AMR][1000 genomes] |
rs10862660 | 0.89[AMR][1000 genomes] |
rs10862672 | 0.86[AMR][1000 genomes] |
rs11115744 | 0.86[AMR][1000 genomes] |
rs11115754 | 0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs11115756 | 0.89[AMR][1000 genomes] |
rs11115872 | 0.86[AMR][1000 genomes] |
rs1490427 | 0.84[ASN][1000 genomes] |
rs1844619 | 0.83[AFR][1000 genomes];0.94[AMR][1000 genomes] |
rs2896466 | 0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs4084722 | 0.86[AFR][1000 genomes];0.94[AMR][1000 genomes] |
rs7136633 | 0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7964484 | 0.84[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv521849 | chr12:83013783-83991479 | Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
2 | nsv1042674 | chr12:83620899-83942628 | Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | esv2755360 | chr12:83843007-83857774 | Enhancers Weak transcription | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:83848000-83857000 | Weak transcription | Fetal Heart | heart |