Variant report
Variant | rs12421556 |
---|---|
Chromosome Location | chr11:57808636-57808637 |
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] |
---|---|
rs12417338 | 0.86[ASN][1000 genomes] |
rs12418614 | 0.81[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs17458061 | 0.95[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs2175276 | 0.86[ASN][1000 genomes] |
rs2866831 | 0.95[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs55665208 | 0.95[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs56023680 | 0.95[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs56245847 | 0.81[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs61903961 | 0.81[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs61903969 | 0.95[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs61904010 | 0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61904013 | 0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61904025 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61904041 | 0.83[EUR][1000 genomes] |
rs61905316 | 0.86[ASN][1000 genomes] |
rs61905341 | 0.86[ASN][1000 genomes] |
rs61905342 | 0.86[ASN][1000 genomes] |
rs61905343 | 0.86[ASN][1000 genomes] |
rs61905344 | 0.80[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs61905345 | 0.80[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs7108167 | 0.86[ASN][1000 genomes] |
rs7112942 | 0.95[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs7128781 | 0.95[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72915744 | 0.82[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72917859 | 0.95[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72919837 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7925491 | 0.86[ASN][1000 genomes] |
rs7944888 | 0.82[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs7945120 | 0.84[EUR][1000 genomes];0.86[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1044030 | chr11:57073395-58035564 | Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 136 gene(s) | inside rSNPs | diseases |
2 | nsv541047 | chr11:57073395-58035564 | Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 136 gene(s) | inside rSNPs | diseases |
3 | nsv1054205 | chr11:57544264-58358509 | Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 67 gene(s) | inside rSNPs | diseases |
4 | nsv897589 | chr11:57623815-58052357 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 24 gene(s) | inside rSNPs | diseases |
5 | esv2761678 | chr11:57768288-57810886 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandlncRNA | 5 gene(s) | inside rSNPs | diseases |
6 | nsv832165 | chr11:57806024-58009076 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:57792000-57811400 | Weak transcription | Right Atrium | heart |
2 | chr11:57808200-57809000 | Enhancers | Pancreas | Pancrea |
3 | chr11:57808400-57809000 | ZNF genes & repeats | Lung | lung |
4 | chr11:57808600-57809000 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |