Variant report
Variant | rs2799344 |
---|---|
Chromosome Location | chr13:53665737-53665738 |
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] |
---|---|
rs12864008 | 0.82[ASN][1000 genomes] |
rs12865218 | 0.87[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12866736 | 0.82[ASN][1000 genomes] |
rs12867491 | 0.85[EUR][1000 genomes] |
rs12868253 | 0.82[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12869523 | 0.85[EUR][1000 genomes] |
rs12870777 | 0.85[EUR][1000 genomes] |
rs12871248 | 0.85[EUR][1000 genomes] |
rs12874939 | 0.85[EUR][1000 genomes] |
rs12876105 | 0.85[EUR][1000 genomes] |
rs12876387 | 0.87[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs12876786 | 0.82[EUR][1000 genomes] |
rs12877178 | 0.87[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12877599 | 0.85[EUR][1000 genomes] |
rs12877758 | 0.85[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs12877912 | 0.82[EUR][1000 genomes] |
rs1343608 | 0.85[EUR][1000 genomes] |
rs17053844 | 0.85[JPT][hapmap];0.83[ASN][1000 genomes] |
rs17053849 | 0.85[JPT][hapmap];0.83[ASN][1000 genomes] |
rs17053872 | 0.83[ASN][1000 genomes] |
rs17054812 | 0.85[EUR][1000 genomes] |
rs17054937 | 0.82[EUR][1000 genomes] |
rs1891947 | 0.82[ASN][1000 genomes] |
rs2799345 | 1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs34030659 | 0.85[EUR][1000 genomes] |
rs34031649 | 0.85[EUR][1000 genomes] |
rs34059997 | 0.85[EUR][1000 genomes] |
rs34110102 | 0.82[ASN][1000 genomes] |
rs34163916 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs34201111 | 0.85[EUR][1000 genomes] |
rs34211399 | 0.87[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs34298498 | 0.87[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs34330988 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs34374288 | 0.82[ASN][1000 genomes] |
rs34531708 | 0.85[EUR][1000 genomes] |
rs34557321 | 0.82[EUR][1000 genomes] |
rs34642277 | 0.87[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs34687272 | 0.85[EUR][1000 genomes] |
rs34708622 | 0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs34756826 | 0.82[EUR][1000 genomes] |
rs34902019 | 0.85[EUR][1000 genomes] |
rs35003538 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs35007240 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs35114755 | 0.85[EUR][1000 genomes] |
rs35121580 | 0.82[ASN][1000 genomes] |
rs35226075 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs35340650 | 0.82[EUR][1000 genomes] |
rs35397855 | 0.83[ASN][1000 genomes] |
rs35472513 | 0.83[ASN][1000 genomes] |
rs35575822 | 0.87[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs35625606 | 0.87[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs35666947 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs35727089 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs35756659 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs35765587 | 0.87[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs35800707 | 0.82[EUR][1000 genomes] |
rs36081995 | 0.82[ASN][1000 genomes] |
rs55972529 | 0.85[EUR][1000 genomes] |
rs57273256 | 0.85[EUR][1000 genomes] |
rs57454139 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs59297590 | 0.85[EUR][1000 genomes] |
rs59345770 | 0.82[ASN][1000 genomes] |
rs59513810 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs59960345 | 0.85[EUR][1000 genomes] |
rs60408242 | 0.85[EUR][1000 genomes] |
rs61950074 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs61950079 | 0.85[EUR][1000 genomes] |
rs61950086 | 0.85[EUR][1000 genomes] |
rs61950491 | 0.82[ASN][1000 genomes] |
rs61950492 | 0.83[ASN][1000 genomes] |
rs61950504 | 0.87[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs61950522 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs6561705 | 0.80[EUR][1000 genomes] |
rs6561706 | 0.85[EUR][1000 genomes] |
rs6561707 | 0.85[EUR][1000 genomes] |
rs7320513 | 0.85[EUR][1000 genomes] |
rs74086489 | 0.87[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7998204 | 0.85[EUR][1000 genomes] |
rs9563136 | 0.82[EUR][1000 genomes] |
rs9563137 | 0.82[EUR][1000 genomes] |
rs9563138 | 0.82[EUR][1000 genomes] |
rs9568814 | 0.82[EUR][1000 genomes] |
rs9568815 | 0.82[EUR][1000 genomes] |
rs9568816 | 0.82[EUR][1000 genomes] |
rs9568817 | 0.82[EUR][1000 genomes] |
rs9568820 | 0.82[EUR][1000 genomes] |
rs9568821 | 0.82[EUR][1000 genomes] |
rs9568822 | 0.82[EUR][1000 genomes] |
rs9568823 | 0.82[EUR][1000 genomes] |
rs9568824 | 0.82[EUR][1000 genomes] |
rs9568825 | 0.82[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv530719 | chr13:53173014-53675953 | Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 26 gene(s) | inside rSNPs | diseases |
2 | esv3440613 | chr13:53307609-53671072 | Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
3 | nsv832613 | chr13:53524319-53687188 | Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:53658600-53666000 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
2 | chr13:53664200-53665800 | Enhancers | Fetal Heart | heart |
3 | chr13:53664200-53666000 | Enhancers | Brain Germinal Matrix | brain |
4 | chr13:53664600-53667000 | Weak transcription | Brain Cingulate Gyrus | brain |
5 | chr13:53664800-53665800 | Weak transcription | Brain Substantia Nigra | brain |
6 | chr13:53665000-53666800 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
7 | chr13:53665000-53667000 | Weak transcription | Brain Angular Gyrus | brain |
8 | chr13:53665200-53667000 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
9 | chr13:53665200-53667000 | Weak transcription | Brain Hippocampus Middle | brain |
10 | chr13:53665600-53667000 | Weak transcription | Pancreas | Pancrea |