Variant report
Variant | rs10093773 |
---|---|
Chromosome Location | chr8:65243151-65243152 |
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 |
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No data |
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No data |
rs_ID | r2[population] |
---|---|
rs10087386 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10090207 | 0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs10097129 | 0.90[EUR][1000 genomes] |
rs10097471 | 0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10099867 | 0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10101906 | 0.95[ASN][1000 genomes] |
rs10103220 | 0.81[EUR][1000 genomes] |
rs10104164 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10105633 | 0.87[EUR][1000 genomes] |
rs10957306 | 0.87[EUR][1000 genomes] |
rs12334830 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12335124 | 0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12708021 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13252463 | 0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs13252892 | 0.88[EUR][1000 genomes] |
rs13254698 | 0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13262851 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13274668 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13275299 | 0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1371684 | 0.86[EUR][1000 genomes] |
rs1371685 | 0.86[EUR][1000 genomes] |
rs1440135 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1440136 | 0.91[EUR][1000 genomes] |
rs1440137 | 0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs16931063 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17223648 | 0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17314320 | 0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs17315206 | 0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1899048 | 0.83[ASN][1000 genomes] |
rs2008156 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2009633 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28631026 | 0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28643545 | 0.89[EUR][1000 genomes] |
rs28875492 | 0.81[EUR][1000 genomes] |
rs28895626 | 0.88[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs4478613 | 0.87[EUR][1000 genomes] |
rs62521215 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62521216 | 0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs67633283 | 0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7822866 | 0.90[EUR][1000 genomes] |
rs7841666 | 0.91[EUR][1000 genomes] |
rs971236 | 0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948343 | chr8:64804219-65328394 | Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 7 gene(s) | inside rSNPs | diseases |
2 | 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 |
3 | esv2761224 | chr8:65235506-65259631 | Weak transcription ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv1830069 | chr8:65235506-65263721 | Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv1031877 | chr8:65240464-65291136 | Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers | TF binding regionCpG islandlncRNA | 7 gene(s) | inside rSNPs | diseases |
6 | esv1808745 | chr8:65242166-65256119 | Enhancers Weak transcription Strong transcription Bivalent Enhancer | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
7 | esv1808838 | chr8:65242166-65256119 | Bivalent Enhancer Enhancers Weak transcription Strong transcription | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
8 | esv1809447 | chr8:65242166-65256119 | Enhancers Strong transcription Bivalent Enhancer Weak transcription | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
9 | esv1812391 | chr8:65242166-65256119 | Strong transcription Enhancers Weak transcription Bivalent Enhancer | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
10 | esv1809961 | chr8:65242166-65268559 | Weak transcription Strong transcription Enhancers Bivalent Enhancer | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
11 | esv1809415 | chr8:65242166-65272478 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
12 | esv1808102 | chr8:65242198-65256379 | Weak transcription Enhancers Strong transcription Bivalent Enhancer | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
13 | nsv6230 | chr8:65242569-65273236 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:65236400-65248000 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |