Variant report
Variant | rs59960294 |
---|---|
Chromosome Location | chr5:118215856-118215857 |
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] |
---|---|
rs17144674 | 1.00[EUR][1000 genomes] |
rs17144719 | 1.00[EUR][1000 genomes] |
rs17144749 | 1.00[EUR][1000 genomes] |
rs17144777 | 1.00[EUR][1000 genomes] |
rs17144807 | 1.00[EUR][1000 genomes] |
rs17144815 | 1.00[EUR][1000 genomes] |
rs56253801 | 1.00[EUR][1000 genomes] |
rs57269254 | 1.00[EUR][1000 genomes] |
rs57626866 | 1.00[EUR][1000 genomes] |
rs57879671 | 1.00[EUR][1000 genomes] |
rs57935306 | 1.00[EUR][1000 genomes] |
rs58272882 | 1.00[EUR][1000 genomes] |
rs58306431 | 1.00[EUR][1000 genomes] |
rs58511548 | 1.00[EUR][1000 genomes] |
rs58532063 | 1.00[EUR][1000 genomes] |
rs58554745 | 0.93[AFR][1000 genomes] |
rs58886471 | 1.00[EUR][1000 genomes] |
rs58907676 | 1.00[EUR][1000 genomes] |
rs59816467 | 1.00[EUR][1000 genomes] |
rs59983556 | 1.00[EUR][1000 genomes] |
rs59989728 | 1.00[EUR][1000 genomes] |
rs60221161 | 1.00[EUR][1000 genomes] |
rs60664847 | 0.88[AFR][1000 genomes] |
rs61128026 | 1.00[EUR][1000 genomes] |
rs61196104 | 1.00[EUR][1000 genomes] |
rs61466105 | 0.88[AFR][1000 genomes] |
rs73236928 | 1.00[EUR][1000 genomes] |
rs73236931 | 1.00[EUR][1000 genomes] |
rs73236933 | 0.86[AFR][1000 genomes] |
rs73236934 | 1.00[EUR][1000 genomes] |
rs73236935 | 0.86[AFR][1000 genomes] |
rs73236937 | 0.86[AFR][1000 genomes] |
rs73236952 | 1.00[EUR][1000 genomes] |
rs73236955 | 1.00[EUR][1000 genomes] |
rs73236956 | 1.00[EUR][1000 genomes] |
rs73236981 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73239013 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73239017 | 1.00[EUR][1000 genomes] |
rs73239018 | 1.00[EUR][1000 genomes] |
rs73239038 | 1.00[EUR][1000 genomes] |
rs73239043 | 1.00[EUR][1000 genomes] |
rs73239050 | 1.00[EUR][1000 genomes] |
rs73239054 | 1.00[EUR][1000 genomes] |
rs73239060 | 0.80[AFR][1000 genomes] |
rs73239061 | 1.00[EUR][1000 genomes] |
rs73239070 | 1.00[EUR][1000 genomes] |
rs73239073 | 1.00[EUR][1000 genomes] |
rs73253504 | 1.00[EUR][1000 genomes] |
rs865396 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv882767 | chr5:117931730-118385691 | Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 21 gene(s) | inside rSNPs | diseases |
2 | nsv599562 | chr5:118122504-118230640 | Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv882771 | chr5:118170135-118230640 | Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv882772 | chr5:118173127-118230640 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | nsv882773 | chr5:118175640-118241854 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv599563 | chr5:118191798-118241854 | Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | nsv526318 | chr5:118210835-118221589 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:118209800-118218000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr5:118214600-118216000 | ZNF genes & repeats | HUES6 Cell Line | embryonic stem cell |
3 | chr5:118215000-118216000 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |