Variant report
Variant | rs475053 |
---|---|
Chromosome Location | chr11:63157540-63157541 |
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] |
---|---|
rs11820135 | 1.00[EUR][1000 genomes] |
rs501594 | 1.00[EUR][1000 genomes] |
rs507893 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55813757 | 1.00[EUR][1000 genomes] |
rs56867396 | 1.00[EUR][1000 genomes] |
rs57247740 | 1.00[EUR][1000 genomes] |
rs57518967 | 1.00[EUR][1000 genomes] |
rs577327 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs597483 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60168208 | 1.00[EUR][1000 genomes] |
rs60590185 | 1.00[EUR][1000 genomes] |
rs60645099 | 1.00[EUR][1000 genomes] |
rs607277 | 0.81[AMR][1000 genomes] |
rs61997169 | 1.00[EUR][1000 genomes] |
rs655995 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs684396 | 0.81[AMR][1000 genomes] |
rs7103797 | 1.00[EUR][1000 genomes] |
rs7123161 | 1.00[EUR][1000 genomes] |
rs7128461 | 1.00[EUR][1000 genomes] |
rs7935128 | 1.00[EUR][1000 genomes] |
rs7939687 | 1.00[EUR][1000 genomes] |
rs7942307 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1051171 | chr11:62987064-63835715 | Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 100 gene(s) | inside rSNPs | diseases |
2 | nsv1053585 | chr11:63057767-63180308 | Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv555178 | chr11:63078742-63197930 | Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv1822068 | chr11:63146055-63239984 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:63155600-63162800 | Weak transcription | Liver | Liver |