Variant report
Variant | rs35372447 |
---|---|
Chromosome Location | chr17:17520672-17520673 |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs11650499 | 1.00[ASN][1000 genomes] |
rs11869600 | 0.80[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs11871738 | 0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12937108 | 0.80[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs12937187 | 0.80[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs12939297 | 0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12939598 | 0.91[ASN][1000 genomes] |
rs12941217 | 0.80[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs12942708 | 0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12943416 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12945496 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12946063 | 0.80[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs12946845 | 0.91[ASN][1000 genomes] |
rs12947517 | 0.85[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12949039 | 0.91[ASN][1000 genomes] |
rs12949336 | 0.91[ASN][1000 genomes] |
rs12950093 | 0.91[ASN][1000 genomes] |
rs12951181 | 0.80[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs12951347 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs12952281 | 0.91[ASN][1000 genomes] |
rs12952629 | 0.80[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs34664666 | 0.91[ASN][1000 genomes] |
rs35660942 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs35851484 | 0.91[ASN][1000 genomes] |
rs58251514 | 0.86[EUR][1000 genomes] |
rs62066210 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9911672 | 0.94[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv907748 | chr17:17412032-17782404 | Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 89 gene(s) | inside rSNPs | diseases |
2 | nsv1065270 | chr17:17430116-17823086 | Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 91 gene(s) | inside rSNPs | diseases |
3 | nsv543236 | chr17:17430116-17823086 | Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 91 gene(s) | inside rSNPs | diseases |
4 | nsv833384 | chr17:17491483-17645648 | Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 26 gene(s) | inside rSNPs | diseases |
5 | nsv869118 | chr17:17509896-17599850 | Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr17:17517200-17529400 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
2 | chr17:17517400-17522800 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
3 | chr17:17517400-17522800 | Weak transcription | Monocytes-CD14+_RO01746 | blood |