Variant report
Variant | rs73771488 |
---|---|
Chromosome Location | chr6:126875085-126875086 |
allele | A/C |
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] |
---|---|
rs55638175 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs55693422 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs55748258 | 1.00[AMR][1000 genomes] |
rs55866117 | 1.00[AMR][1000 genomes] |
rs55999742 | 1.00[AMR][1000 genomes] |
rs56949492 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs57495004 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs57768813 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs57815345 | 1.00[AMR][1000 genomes] |
rs58167367 | 1.00[AMR][1000 genomes] |
rs58940730 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs60332165 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73771459 | 1.00[AMR][1000 genomes] |
rs73771462 | 1.00[AMR][1000 genomes] |
rs73771463 | 1.00[AMR][1000 genomes] |
rs73771464 | 1.00[AMR][1000 genomes] |
rs73771466 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73771469 | 1.00[AMR][1000 genomes] |
rs73771471 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73771474 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73771477 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73771482 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73771483 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73771484 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73771486 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73771489 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73771490 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73771499 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73773112 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73773115 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73773119 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73773120 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73773124 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73773128 | 1.00[AMR][1000 genomes] |
rs73773129 | 1.00[AMR][1000 genomes] |
rs73773130 | 1.00[AMR][1000 genomes] |
rs73773131 | 1.00[AMR][1000 genomes] |
rs73773134 | 1.00[AMR][1000 genomes] |
rs73773136 | 1.00[AMR][1000 genomes] |
rs73773137 | 1.00[AMR][1000 genomes] |
rs73773138 | 1.00[AMR][1000 genomes] |
rs73773143 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1021636 | chr6:126792916-127022489 | Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 8 gene(s) | inside rSNPs | diseases |
2 | nsv1026498 | chr6:126812609-127397240 | Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
3 | nsv1024206 | chr6:126873187-127475713 | Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
4 | nsv538438 | chr6:126873187-127475713 | Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
5 | esv3413206 | chr6:126874609-126876907 | Enhancers Weak transcription | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:126872200-126880000 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
2 | chr6:126874800-126875200 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |