Variant report
Variant | rs16914414 |
---|---|
Chromosome Location | chr8:51094759-51094760 |
allele | A/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 |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10085950 | 0.85[AMR][1000 genomes] |
rs10096911 | 0.83[AMR][1000 genomes] |
rs10097416 | 0.83[AMR][1000 genomes] |
rs10098450 | 0.85[AMR][1000 genomes] |
rs10100515 | 0.91[YRI][hapmap];1.00[AMR][1000 genomes] |
rs10107442 | 1.00[AMR][1000 genomes] |
rs10109132 | 0.83[AMR][1000 genomes] |
rs10113626 | 0.85[AMR][1000 genomes] |
rs16914125 | 1.00[AMR][1000 genomes] |
rs16914130 | 1.00[AMR][1000 genomes] |
rs16914334 | 1.00[YRI][hapmap] |
rs16914355 | 0.85[YRI][hapmap] |
rs16914433 | 1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs28418948 | 1.00[AMR][1000 genomes] |
rs28438566 | 0.85[AMR][1000 genomes] |
rs28468445 | 1.00[AMR][1000 genomes] |
rs28524672 | 0.83[AMR][1000 genomes] |
rs28552506 | 0.83[AMR][1000 genomes] |
rs28553511 | 0.85[AMR][1000 genomes] |
rs28557047 | 0.85[AMR][1000 genomes] |
rs28566866 | 0.83[AMR][1000 genomes] |
rs28664922 | 0.90[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs28676677 | 0.83[AMR][1000 genomes] |
rs28784070 | 0.88[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs56234780 | 1.00[AMR][1000 genomes] |
rs58638825 | 0.85[AMR][1000 genomes] |
rs59313993 | 0.85[AMR][1000 genomes] |
rs60600453 | 0.83[AMR][1000 genomes] |
rs61279830 | 1.00[AMR][1000 genomes] |
rs6990200 | 0.85[AMR][1000 genomes] |
rs73569361 | 1.00[AMR][1000 genomes] |
rs73569366 | 1.00[AMR][1000 genomes] |
rs73569370 | 0.83[AMR][1000 genomes] |
rs73569372 | 1.00[AMR][1000 genomes] |
rs73569374 | 1.00[AMR][1000 genomes] |
rs73569385 | 1.00[AMR][1000 genomes] |
rs73573511 | 0.83[AMR][1000 genomes] |
rs73573585 | 0.85[AMR][1000 genomes] |
rs73575345 | 0.83[AMR][1000 genomes] |
rs73575352 | 0.83[AMR][1000 genomes] |
rs73575355 | 0.91[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs73577267 | 0.85[AMR][1000 genomes] |
rs73577275 | 0.85[AMR][1000 genomes] |
rs73579271 | 0.83[AMR][1000 genomes] |
rs73676211 | 0.83[AMR][1000 genomes] |
rs73677828 | 1.00[AMR][1000 genomes] |
rs73677829 | 0.83[AMR][1000 genomes] |
rs7822276 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3353749 | chr8:50530807-51139242 | Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv916392 | chr8:50827638-51395140 | Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | esv2759613 | chr8:50873293-51137995 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv2758621 | chr8:50886593-51137995 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | esv1829361 | chr8:51021638-51101126 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | nsv1027984 | chr8:51060895-51098808 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS | TF binding regionCpG islandlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:51093800-51095400 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
2 | chr8:51094000-51095400 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |