Variant report
Variant | rs7218682 |
---|---|
Chromosome Location | chr17:16860191-16860192 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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(count:3 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs10468462 | 0.86[ASN][1000 genomes] |
rs10468463 | 0.84[ASN][1000 genomes] |
rs11078360 | 0.97[AFR][1000 genomes] |
rs11078361 | 0.97[AFR][1000 genomes] |
rs12051726 | 0.93[AFR][1000 genomes] |
rs12051889 | 0.93[AFR][1000 genomes] |
rs12051890 | 0.93[AFR][1000 genomes] |
rs12051892 | 0.93[AFR][1000 genomes] |
rs12051899 | 0.97[AFR][1000 genomes] |
rs12051900 | 0.97[AFR][1000 genomes] |
rs12150243 | 0.95[AFR][1000 genomes] |
rs12325872 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34870066 | 0.93[AFR][1000 genomes] |
rs35678976 | 0.97[AFR][1000 genomes] |
rs4985783 | 0.82[ASN][1000 genomes] |
rs56369903 | 0.94[ASN][1000 genomes] |
rs66479858 | 0.93[AFR][1000 genomes] |
rs66847673 | 0.93[AFR][1000 genomes] |
rs67001256 | 0.93[AFR][1000 genomes] |
rs7214221 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7216399 | 0.82[ASN][1000 genomes] |
rs7222430 | 0.84[ASN][1000 genomes] |
rs73980239 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73980240 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73980241 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs8082017 | 0.93[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1058448 | chr17:16389870-16926287 | Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 53 gene(s) | inside rSNPs | diseases |
2 | nsv1055688 | chr17:16800788-16868860 | Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv1058863 | chr17:16812121-16943780 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
4 | nsv543227 | chr17:16812121-16943780 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
5 | nsv907726 | chr17:16821204-16875636 | Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr17:16856400-16860400 | Genic enhancers | Primary B cells from peripheral blood | blood |
2 | chr17:16859200-16862000 | Transcr. at gene 5' and 3' | GM12878-XiMat | blood |
3 | chr17:16859400-16860400 | Enhancers | Primary B cells from cord blood | blood |