Variant report
Variant | rs2030009 |
---|---|
Chromosome Location | chr6:28007419-28007420 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
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(count:2 , 50 per page) page:
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Variant related genes | Relation type |
---|---|
ENSG00000196331 | Chromatin interaction |
ENSG00000233224 | Chromatin interaction |
ENSG00000197153 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1529749 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17708949 | 0.84[ASN][1000 genomes] |
rs17709097 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs17709109 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17709523 | 0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs17765491 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs2030008 | 1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2394044 | 1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9348785 | 0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs9357055 | 0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs9357056 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9357057 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs9357059 | 0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs9368545 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9380034 | 1.00[AFR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9380038 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9380039 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9393873 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9393874 | 1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9393879 | 0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv432858 | chr6:27719375-28011652 | Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 387 gene(s) | inside rSNPs | diseases |
2 | nsv1022651 | chr6:27864217-28017997 | Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 50 gene(s) | inside rSNPs | diseases |
3 | nsv830619 | chr6:27872302-28062544 | Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 38 gene(s) | inside rSNPs | diseases |
4 | nsv883513 | chr6:27982152-28033087 | Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
5 | esv1817841 | chr6:27984907-28007435 | Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 7 gene(s) | inside rSNPs | diseases |
6 | nsv981052 | chr6:27987196-28024382 | Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 12 gene(s) | inside rSNPs | diseases |
No data |