Variant report
Variant | rs73689578 |
---|---|
Chromosome Location | chr8:65634731-65634732 |
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] |
---|---|
rs12674544 | 1.00[ASN][1000 genomes] |
rs12682028 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs16931374 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs3779871 | 1.00[ASN][1000 genomes] |
rs41333745 | 1.00[ASN][1000 genomes] |
rs4263804 | 1.00[ASN][1000 genomes] |
rs4358837 | 1.00[ASN][1000 genomes] |
rs4437695 | 1.00[ASN][1000 genomes] |
rs4521800 | 1.00[ASN][1000 genomes] |
rs4543580 | 1.00[ASN][1000 genomes] |
rs4737202 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs4737677 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs4737684 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs55816857 | 1.00[ASN][1000 genomes] |
rs55839813 | 1.00[ASN][1000 genomes] |
rs56136042 | 1.00[ASN][1000 genomes] |
rs56345307 | 1.00[ASN][1000 genomes] |
rs56378428 | 1.00[ASN][1000 genomes] |
rs56682216 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs56822105 | 1.00[ASN][1000 genomes] |
rs57071798 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs57148757 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs57198819 | 1.00[ASN][1000 genomes] |
rs57241952 | 1.00[ASN][1000 genomes] |
rs57696702 | 1.00[ASN][1000 genomes] |
rs57948164 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs58284770 | 1.00[ASN][1000 genomes] |
rs58303167 | 1.00[ASN][1000 genomes] |
rs58420338 | 1.00[ASN][1000 genomes] |
rs58451406 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs58603842 | 1.00[ASN][1000 genomes] |
rs58668371 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs58740344 | 1.00[ASN][1000 genomes] |
rs59556318 | 1.00[ASN][1000 genomes] |
rs59928224 | 1.00[ASN][1000 genomes] |
rs60034994 | 1.00[ASN][1000 genomes] |
rs60347741 | 1.00[ASN][1000 genomes] |
rs60551204 | 1.00[ASN][1000 genomes] |
rs61078378 | 1.00[ASN][1000 genomes] |
rs7012812 | 1.00[ASN][1000 genomes] |
rs73237769 | 1.00[ASN][1000 genomes] |
rs73237778 | 1.00[ASN][1000 genomes] |
rs73244630 | 1.00[ASN][1000 genomes] |
rs73688006 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73688014 | 1.00[ASN][1000 genomes] |
rs73688018 | 1.00[ASN][1000 genomes] |
rs73688019 | 1.00[ASN][1000 genomes] |
rs73688022 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73688023 | 1.00[ASN][1000 genomes] |
rs73688285 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73688286 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73688288 | 1.00[ASN][1000 genomes] |
rs73688289 | 1.00[ASN][1000 genomes] |
rs73688293 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73688294 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73688300 | 1.00[ASN][1000 genomes] |
rs73688301 | 1.00[ASN][1000 genomes] |
rs73689569 | 1.00[ASN][1000 genomes] |
rs73689574 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73689575 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs7831851 | 1.00[ASN][1000 genomes] |
rs9918785 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv534001 | chr8:64992196-65798776 | Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 17 gene(s) | inside rSNPs | diseases |
2 | esv2761434 | chr8:65578467-66567678 | Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:65632400-65634800 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
2 | chr8:65634600-65635000 | Enhancers | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
3 | chr8:65634600-65635000 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
4 | chr8:65634600-65636000 | Enhancers | Brain Hippocampus Middle | brain |