Variant report
Variant | rs73441857 |
---|---|
Chromosome Location | chr6:49712320-49712321 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:22)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:22 , 50 per page) page:
1
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | FOSL2 | chr6:49711989-49712373 | MCF-7 | breast: | n/a | n/a |
2 | FOS | chr6:49712021-49712375 | MCF10A-Er-Src | breast: | n/a | n/a |
3 | STAT3 | chr6:49711922-49712326 | MCF10A-Er-Src | breast: | n/a | n/a |
4 | FOS | chr6:49712033-49712445 | MCF10A-Er-Src | breast: | n/a | n/a |
5 | NR2F2 | chr6:49711942-49712324 | MCF-7 | breast: | n/a | n/a |
6 | FOS | chr6:49712038-49712355 | MCF10A-Er-Src | breast: | n/a | n/a |
7 | ARID3A | chr6:49712049-49712395 | K562 | blood: | n/a | n/a |
8 | STAT3 | chr6:49712072-49712328 | MCF10A-Er-Src | breast: | n/a | n/a |
9 | CEBPB | chr6:49712010-49712367 | MCF-7 | breast: | n/a | chr6:49712161-49712172 chr6:49712160-49712171 |
10 | JUN | chr6:49712273-49712616 | K562 | blood: | n/a | n/a |
11 | EP300 | chr6:49712020-49712359 | Hela-S3 | cervix: | n/a | chr6:49712139-49712148 |
12 | GATA3 | chr6:49712007-49712339 | T-47D | breast: | n/a | chr6:49712137-49712147 |
13 | MYC | chr6:49712024-49712325 | MCF10A-Er-Src | breast: | n/a | n/a |
14 | CEBPB | chr6:49711989-49712396 | Hela-S3 | cervix: | n/a | chr6:49712161-49712172 chr6:49712160-49712171 |
15 | FOS | chr6:49712052-49712348 | MCF10A-Er-Src | breast: | n/a | n/a |
16 | ELF1 | chr6:49711857-49712420 | MCF-7 | breast: | n/a | chr6:49712139-49712150 |
17 | E2F4 | chr6:49712126-49712348 | MCF10A-Er-Src | breast: | n/a | n/a |
18 | CEBPB | chr6:49711925-49712439 | MCF-7 | breast: | n/a | chr6:49712161-49712172 chr6:49712160-49712171 |
19 | POLR2A | chr6:49712283-49712625 | K562 | blood: | n/a | n/a |
20 | FOXA1 | chr6:49711979-49712344 | T-47D | breast: | n/a | n/a |
21 | FOXA1 | chr6:49711933-49712434 | HepG2 | liver: | n/a | n/a |
22 | SIN3AK20 | chr6:49711815-49712444 | MCF-7 | breast: | n/a | n/a |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
CRISP3 | TF binding region |
ENSG00000096006 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10948530 | 1.00[EUR][1000 genomes] |
rs12111232 | 1.00[EUR][1000 genomes] |
rs1268283 | 1.00[EUR][1000 genomes] |
rs1268284 | 1.00[EUR][1000 genomes] |
rs1268286 | 1.00[EUR][1000 genomes] |
rs1268797 | 1.00[EUR][1000 genomes] |
rs1270361 | 1.00[EUR][1000 genomes] |
rs1383377 | 1.00[EUR][1000 genomes] |
rs16879837 | 1.00[EUR][1000 genomes] |
rs2396908 | 1.00[EUR][1000 genomes] |
rs28553529 | 1.00[EUR][1000 genomes] |
rs35289289 | 1.00[EUR][1000 genomes] |
rs4504474 | 1.00[AMR][1000 genomes] |
rs56994564 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57160213 | 1.00[EUR][1000 genomes] |
rs57245652 | 1.00[EUR][1000 genomes] |
rs57254982 | 1.00[EUR][1000 genomes] |
rs57295760 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57341323 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57400170 | 1.00[EUR][1000 genomes] |
rs57420263 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57746041 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57968495 | 1.00[EUR][1000 genomes] |
rs58055962 | 1.00[EUR][1000 genomes] |
rs58116328 | 1.00[EUR][1000 genomes] |
rs58662430 | 1.00[EUR][1000 genomes] |
rs58946005 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59244495 | 1.00[EUR][1000 genomes] |
rs59784644 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59924621 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60493453 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60504565 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60669025 | 1.00[EUR][1000 genomes] |
rs60925322 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61041053 | 1.00[EUR][1000 genomes] |
rs61041067 | 1.00[EUR][1000 genomes] |
rs61273820 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61554370 | 0.83[AMR][1000 genomes] |
rs61627916 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6458700 | 1.00[EUR][1000 genomes] |
rs6458703 | 1.00[EUR][1000 genomes] |
rs6919805 | 1.00[EUR][1000 genomes] |
rs73423739 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73425837 | 1.00[EUR][1000 genomes] |
rs73425844 | 1.00[EUR][1000 genomes] |
rs73425861 | 1.00[EUR][1000 genomes] |
rs73425868 | 1.00[EUR][1000 genomes] |
rs73425873 | 1.00[EUR][1000 genomes] |
rs73425895 | 1.00[EUR][1000 genomes] |
rs73425899 | 1.00[EUR][1000 genomes] |
rs73427869 | 1.00[EUR][1000 genomes] |
rs73433897 | 1.00[EUR][1000 genomes] |
rs73435808 | 1.00[EUR][1000 genomes] |
rs73435811 | 1.00[EUR][1000 genomes] |
rs73435814 | 1.00[EUR][1000 genomes] |
rs73435828 | 1.00[EUR][1000 genomes] |
rs73435837 | 1.00[EUR][1000 genomes] |
rs73435853 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73435867 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73435869 | 1.00[EUR][1000 genomes] |
rs73435872 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73435876 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73435899 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73435901 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73437803 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73437853 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73437860 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73437864 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73437867 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73437871 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73437872 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73437876 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73437878 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73437880 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73437882 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73437884 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73439848 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73439854 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73439856 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73439857 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73439862 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73439865 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73439869 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73439877 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73441811 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73441829 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73441834 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73441836 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73441840 | 0.83[AMR][1000 genomes];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 |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:49711400-49713000 | Enhancers | Primary neutrophils fromperipheralblood | blood |
2 | chr6:49712200-49714200 | Weak transcription | K562 | blood |