Variant report
Variant | rs3877190 |
---|---|
Chromosome Location | chr18:14986956-14986957 |
allele | A/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 |
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No data |
No data |
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No data |
rs_ID | r2[population] |
---|---|
rs12959896 | 0.90[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs12964743 | 0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12968377 | 0.90[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs12969097 | 0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs1829374 | 0.93[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs1878802 | 0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs1976777 | 0.93[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs28481769 | 0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs28524777 | 0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs3889355 | 0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs4243282 | 0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs4890740 | 0.91[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs4890741 | 0.93[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs56752121 | 0.90[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7230084 | 0.92[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs7233093 | 0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7237724 | 0.91[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs8093953 | 0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs9946841 | 0.94[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs9947258 | 0.93[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs9950732 | 0.90[EUR][1000 genomes];0.85[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv916419 | chr18:14418522-15165372 | Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 27 gene(s) | inside rSNPs | diseases |
2 | esv2751771 | chr18:14704694-15106727 | Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 18 gene(s) | inside rSNPs | diseases |
3 | nsv909434 | chr18:14841828-15149366 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
4 | esv33381 | chr18:14929347-15052868 | Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | nsv576543 | chr18:14949001-15178340 | Active TSS Bivalent/Poised TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
6 | esv2761993 | chr18:14956916-15402408 | Bivalent Enhancer ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
7 | nsv960266 | chr18:14984974-14987575 | Weak transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
8 | nsv960265 | chr18:14984974-14991119 | Enhancers Weak transcription | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr18:14985400-14988400 | Enhancers | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
2 | chr18:14986600-14987000 | Enhancers | Adipose Nuclei | Adipose |