Variant report
Variant | rs9930102 |
---|---|
Chromosome Location | chr16:71530208-71530209 |
allele | C/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)
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(count:2 , 50 per page) page:
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Variant related genes | Relation type |
---|---|
ENSG00000167377 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs13330287 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs13331410 | 0.87[AMR][1000 genomes] |
rs13337117 | 0.83[AFR][1000 genomes] |
rs16973245 | 0.88[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs28537877 | 0.87[AMR][1000 genomes] |
rs28653370 | 0.86[AFR][1000 genomes] |
rs28676959 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs28754484 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs57343221 | 1.00[AMR][1000 genomes] |
rs7194638 | 0.87[YRI][hapmap] |
rs73573696 | 0.87[AMR][1000 genomes] |
rs73575922 | 0.87[AMR][1000 genomes] |
rs9923065 | 0.91[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs9927819 | 1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs9930642 | 0.96[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs9933647 | 0.84[AFR][1000 genomes] |
rs9939096 | 0.83[AFR][1000 genomes] |
rs9940204 | 0.88[YRI][hapmap];0.87[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949461 | chr16:71196153-71579711 | ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 41 gene(s) | inside rSNPs | diseases |
2 | nsv906892 | chr16:71526720-71570413 | Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |