Variant report
Variant | rs73425868 |
---|---|
Chromosome Location | chr6:49818102-49818103 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:6)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:6 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr6:49597656..49601236-chr6:49815948..49819528,4 | K562 | blood: | |
2 | chr6:49817546..49820511-chr6:49881787..49884354,2 | MCF-7 | breast: | |
3 | chr6:49499080..49500519-chr6:49816228..49818102,14 | K562 | blood: | |
4 | chr6:49608680..49611056-chr6:49815875..49818691,2 | K562 | blood: | |
5 | chr6:49817615..49819181-chr6:49819234..49821826,2 | K562 | blood: | |
6 | chr6:49522660..49524598-chr6:49816309..49818376,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10948530 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12111232 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16879837 | 1.00[EUR][1000 genomes] |
rs28553529 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28738068 | 1.00[EUR][1000 genomes] |
rs35289289 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56994564 | 1.00[EUR][1000 genomes] |
rs57160213 | 1.00[EUR][1000 genomes] |
rs57245652 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57254982 | 1.00[EUR][1000 genomes] |
rs57295760 | 1.00[EUR][1000 genomes] |
rs57341323 | 1.00[EUR][1000 genomes] |
rs57400170 | 1.00[EUR][1000 genomes] |
rs57420263 | 1.00[EUR][1000 genomes] |
rs57746041 | 1.00[EUR][1000 genomes] |
rs57789146 | 0.81[AFR][1000 genomes] |
rs58055962 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58116328 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58662430 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58946005 | 1.00[EUR][1000 genomes] |
rs59244495 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59713335 | 1.00[EUR][1000 genomes] |
rs59784644 | 1.00[EUR][1000 genomes] |
rs59924621 | 1.00[EUR][1000 genomes] |
rs60493453 | 1.00[EUR][1000 genomes] |
rs60504565 | 1.00[EUR][1000 genomes] |
rs60925322 | 1.00[EUR][1000 genomes] |
rs61041053 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61041067 | 1.00[EUR][1000 genomes] |
rs61273820 | 1.00[EUR][1000 genomes] |
rs61627916 | 1.00[EUR][1000 genomes] |
rs6919805 | 1.00[EUR][1000 genomes] |
rs73423739 | 1.00[EUR][1000 genomes] |
rs73425837 | 0.81[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73425844 | 1.00[EUR][1000 genomes] |
rs73425861 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73425873 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73425895 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73425899 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73427869 | 1.00[EUR][1000 genomes] |
rs73435853 | 1.00[EUR][1000 genomes] |
rs73435867 | 1.00[EUR][1000 genomes] |
rs73435869 | 1.00[EUR][1000 genomes] |
rs73435872 | 1.00[EUR][1000 genomes] |
rs73435876 | 1.00[EUR][1000 genomes] |
rs73435899 | 1.00[EUR][1000 genomes] |
rs73435901 | 1.00[EUR][1000 genomes] |
rs73437803 | 1.00[EUR][1000 genomes] |
rs73437853 | 1.00[EUR][1000 genomes] |
rs73437860 | 1.00[EUR][1000 genomes] |
rs73437864 | 1.00[EUR][1000 genomes] |
rs73437867 | 1.00[EUR][1000 genomes] |
rs73437871 | 1.00[EUR][1000 genomes] |
rs73437872 | 1.00[EUR][1000 genomes] |
rs73437876 | 1.00[EUR][1000 genomes] |
rs73437878 | 1.00[EUR][1000 genomes] |
rs73437880 | 1.00[EUR][1000 genomes] |
rs73437882 | 1.00[EUR][1000 genomes] |
rs73437884 | 1.00[EUR][1000 genomes] |
rs73439848 | 1.00[EUR][1000 genomes] |
rs73439854 | 1.00[EUR][1000 genomes] |
rs73439856 | 1.00[EUR][1000 genomes] |
rs73439857 | 1.00[EUR][1000 genomes] |
rs73439862 | 1.00[EUR][1000 genomes] |
rs73439865 | 1.00[EUR][1000 genomes] |
rs73439869 | 1.00[EUR][1000 genomes] |
rs73439877 | 1.00[EUR][1000 genomes] |
rs73441811 | 1.00[EUR][1000 genomes] |
rs73441829 | 1.00[EUR][1000 genomes] |
rs73441834 | 1.00[EUR][1000 genomes] |
rs73441836 | 1.00[EUR][1000 genomes] |
rs73441840 | 1.00[EUR][1000 genomes] |
rs73441857 | 1.00[EUR][1000 genomes] |
rs9473702 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv933942 | chr6:49480550-50004231 | Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 25 gene(s) | inside rSNPs | diseases |
2 | nsv933833 | chr6:49515134-49961765 | Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
3 | nsv5294 | chr6:49816788-49853346 | Enhancers Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:49817400-49820200 | Weak transcription | K562 | blood |