Variant report
Variant | rs73411564 |
---|---|
Chromosome Location | chr9:15963020-15963021 |
allele | C/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] |
---|---|
rs12001109 | 1.00[AMR][1000 genomes] |
rs12002511 | 1.00[AMR][1000 genomes] |
rs1328270 | 1.00[AMR][1000 genomes] |
rs1328272 | 1.00[AMR][1000 genomes] |
rs16933906 | 1.00[AMR][1000 genomes] |
rs1857024 | 1.00[AMR][1000 genomes] |
rs1887673 | 1.00[AMR][1000 genomes] |
rs2149232 | 1.00[AMR][1000 genomes] |
rs41439648 | 1.00[AMR][1000 genomes] |
rs56312242 | 1.00[AMR][1000 genomes] |
rs56679179 | 1.00[AMR][1000 genomes] |
rs56774729 | 1.00[AMR][1000 genomes] |
rs57158144 | 1.00[AMR][1000 genomes] |
rs57351686 | 1.00[AMR][1000 genomes] |
rs57779097 | 1.00[AMR][1000 genomes] |
rs58010776 | 1.00[AMR][1000 genomes] |
rs58373606 | 1.00[AMR][1000 genomes] |
rs58603418 | 1.00[AMR][1000 genomes] |
rs58970083 | 1.00[AMR][1000 genomes] |
rs58999162 | 1.00[AMR][1000 genomes] |
rs59106947 | 1.00[AMR][1000 genomes] |
rs59198717 | 1.00[AMR][1000 genomes] |
rs59352577 | 1.00[AMR][1000 genomes] |
rs59574569 | 1.00[AMR][1000 genomes] |
rs59655011 | 1.00[AMR][1000 genomes] |
rs59703985 | 1.00[AMR][1000 genomes] |
rs59860684 | 1.00[AMR][1000 genomes] |
rs59882619 | 1.00[AMR][1000 genomes] |
rs60249192 | 1.00[AMR][1000 genomes] |
rs60322090 | 1.00[AMR][1000 genomes] |
rs60418791 | 1.00[AMR][1000 genomes] |
rs60581753 | 1.00[AMR][1000 genomes] |
rs60641653 | 1.00[AMR][1000 genomes] |
rs60655538 | 1.00[AMR][1000 genomes] |
rs60692567 | 1.00[AMR][1000 genomes] |
rs60846086 | 1.00[AMR][1000 genomes] |
rs61481057 | 1.00[AMR][1000 genomes] |
rs73411539 | 1.00[AMR][1000 genomes] |
rs73411548 | 1.00[AMR][1000 genomes] |
rs73411550 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73411556 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73411562 | 1.00[AMR][1000 genomes] |
rs73411587 | 1.00[AMR][1000 genomes] |
rs73413909 | 1.00[AMR][1000 genomes] |
rs73413926 | 1.00[AMR][1000 genomes] |
rs73413946 | 1.00[AMR][1000 genomes] |
rs73413991 | 1.00[AMR][1000 genomes] |
rs73417830 | 1.00[AMR][1000 genomes] |
rs73418180 | 1.00[AMR][1000 genomes] |
rs73420322 | 1.00[AMR][1000 genomes] |
rs73420371 | 1.00[AMR][1000 genomes] |
rs73420377 | 1.00[AMR][1000 genomes] |
rs73420384 | 1.00[AMR][1000 genomes] |
rs73420388 | 1.00[AMR][1000 genomes] |
rs73422705 | 1.00[AMR][1000 genomes] |
rs73422726 | 1.00[AMR][1000 genomes] |
rs73422740 | 1.00[AMR][1000 genomes] |
rs73422753 | 1.00[AMR][1000 genomes] |
rs73424824 | 1.00[AMR][1000 genomes] |
rs73424825 | 1.00[AMR][1000 genomes] |
rs73424832 | 1.00[AMR][1000 genomes] |
rs73424853 | 1.00[AMR][1000 genomes] |
rs73644957 | 1.00[AMR][1000 genomes] |
rs73644958 | 1.00[AMR][1000 genomes] |
rs73644961 | 1.00[AMR][1000 genomes] |
rs73645248 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv892625 | chr9:15326251-16064850 | Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 35 gene(s) | inside rSNPs | diseases |
2 | esv2753625 | chr9:15914055-15980320 | ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer | lncRNA | n/a | inside rSNPs | diseases |
3 | nsv892637 | chr9:15926508-16060746 | Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:15952600-15987600 | Weak transcription | Primary hematopoietic stem cells | blood |
2 | chr9:15955800-15972600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
3 | chr9:15958400-15972200 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |