Variant report
Variant | rs1918346 |
---|---|
Chromosome Location | chr2:178530560-178530561 |
allele | C/G |
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] |
---|---|
rs10497497 | 0.81[EUR][1000 genomes] |
rs11679730 | 0.82[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs12618150 | 0.93[EUR][1000 genomes] |
rs12620285 | 0.81[EUR][1000 genomes] |
rs13017234 | 0.93[EUR][1000 genomes] |
rs13017429 | 0.89[EUR][1000 genomes] |
rs13025391 | 0.93[EUR][1000 genomes] |
rs13025904 | 0.93[EUR][1000 genomes] |
rs13026012 | 0.93[EUR][1000 genomes] |
rs13028757 | 0.93[EUR][1000 genomes] |
rs1317945 | 0.93[EUR][1000 genomes] |
rs1358326 | 0.93[EUR][1000 genomes] |
rs1358327 | 0.93[EUR][1000 genomes] |
rs1446839 | 0.81[EUR][1000 genomes] |
rs1527403 | 0.86[EUR][1000 genomes] |
rs1534305 | 0.83[EUR][1000 genomes] |
rs1544001 | 0.93[EUR][1000 genomes] |
rs1918345 | 0.85[EUR][1000 genomes] |
rs1918347 | 0.92[EUR][1000 genomes] |
rs1997206 | 0.93[EUR][1000 genomes] |
rs1997207 | 0.85[EUR][1000 genomes] |
rs2091442 | 0.86[EUR][1000 genomes] |
rs2222712 | 0.85[EUR][1000 genomes] |
rs2365620 | 0.93[EUR][1000 genomes] |
rs2365621 | 0.93[EUR][1000 genomes] |
rs4110134 | 0.93[EUR][1000 genomes] |
rs4341975 | 0.93[EUR][1000 genomes] |
rs4893970 | 0.81[EUR][1000 genomes] |
rs4893973 | 0.83[EUR][1000 genomes] |
rs4893978 | 0.93[EUR][1000 genomes] |
rs4893979 | 0.88[EUR][1000 genomes] |
rs5025340 | 0.86[EUR][1000 genomes] |
rs6433685 | 0.93[EUR][1000 genomes] |
rs6433686 | 0.83[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs6433687 | 0.93[EUR][1000 genomes] |
rs6433688 | 0.93[EUR][1000 genomes] |
rs6721360 | 0.93[EUR][1000 genomes] |
rs6723031 | 0.81[EUR][1000 genomes] |
rs6755382 | 0.91[EUR][1000 genomes] |
rs6756918 | 0.81[EUR][1000 genomes] |
rs7560080 | 0.93[EUR][1000 genomes] |
rs7560514 | 0.93[EUR][1000 genomes] |
rs7560737 | 0.93[EUR][1000 genomes] |
rs7573345 | 0.85[EUR][1000 genomes] |
rs7577552 | 0.93[EUR][1000 genomes] |
rs7578901 | 0.93[EUR][1000 genomes] |
rs7586934 | 0.93[EUR][1000 genomes] |
rs7593744 | 0.89[EUR][1000 genomes] |
rs7593753 | 0.82[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs7597640 | 0.93[EUR][1000 genomes] |
rs941271 | 0.93[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv999086 | chr2:178262348-178773585 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 14 gene(s) | inside rSNPs | diseases |
2 | nsv536055 | chr2:178262348-178773585 | Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 14 gene(s) | inside rSNPs | diseases |
3 | nsv583688 | chr2:178427640-178540293 | Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 12 gene(s) | inside rSNPs | diseases |
4 | nsv431812 | chr2:178525371-178584470 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:178517200-178530800 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
2 | chr2:178524800-178532800 | Weak transcription | Fetal Kidney | kidney |
3 | chr2:178524800-178533400 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
4 | chr2:178528600-178534000 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |