Variant report
Variant | rs59518469 |
---|---|
Chromosome Location | chr3:97979027-97979028 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:5)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:5 , 50 per page) page:
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No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | CTCF | chr3:97978980-97979130 | A549 | lung: | n/a | n/a |
2 | POLR2A | chr3:97978932-97979301 | GM12878 | blood: | n/a | n/a |
3 | CTCF | chr3:97978940-97979090 | GM12866 | blood: | n/a | n/a |
4 | CTCF | chr3:97978900-97979050 | Caco-2 | colon: | n/a | n/a |
5 | CTCF | chr3:97978900-97979050 | GM12870 | blood: | n/a | n/a |
No data |
(count:2 , 50 per page) page:
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No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
OR5H6 | TF binding region |
rs_ID | r2[population] |
---|---|
rs1497547 | 1.00[EUR][1000 genomes] |
rs1603598 | 1.00[AMR][1000 genomes] |
rs16839491 | 1.00[EUR][1000 genomes] |
rs1846079 | 1.00[AMR][1000 genomes] |
rs1846080 | 1.00[AMR][1000 genomes] |
rs1846084 | 1.00[EUR][1000 genomes] |
rs1909001 | 1.00[EUR][1000 genomes] |
rs1909002 | 1.00[EUR][1000 genomes] |
rs4358332 | 1.00[EUR][1000 genomes] |
rs4582089 | 1.00[AMR][1000 genomes] |
rs55696575 | 1.00[AMR][1000 genomes] |
rs55985096 | 1.00[AMR][1000 genomes] |
rs56731928 | 1.00[EUR][1000 genomes] |
rs57361363 | 1.00[AMR][1000 genomes] |
rs58415495 | 1.00[AMR][1000 genomes] |
rs59124064 | 1.00[EUR][1000 genomes] |
rs59403104 | 1.00[EUR][1000 genomes] |
rs59879616 | 1.00[EUR][1000 genomes] |
rs60154921 | 1.00[AMR][1000 genomes] |
rs60579668 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60579974 | 1.00[AMR][1000 genomes] |
rs60903056 | 1.00[EUR][1000 genomes] |
rs6786574 | 1.00[EUR][1000 genomes] |
rs72922848 | 1.00[EUR][1000 genomes] |
rs72931085 | 1.00[EUR][1000 genomes] |
rs72932838 | 1.00[EUR][1000 genomes] |
rs72932843 | 0.95[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72932901 | 1.00[EUR][1000 genomes] |
rs72934924 | 1.00[EUR][1000 genomes] |
rs72934931 | 1.00[EUR][1000 genomes] |
rs72934978 | 1.00[EUR][1000 genomes] |
rs72934981 | 1.00[EUR][1000 genomes] |
rs72937126 | 1.00[EUR][1000 genomes] |
rs73854543 | 1.00[EUR][1000 genomes] |
rs73854599 | 1.00[AMR][1000 genomes] |
rs73854600 | 1.00[AMR][1000 genomes] |
rs73854601 | 1.00[AMR][1000 genomes] |
rs73854602 | 1.00[AMR][1000 genomes] |
rs73854623 | 1.00[AMR][1000 genomes] |
rs73854624 | 1.00[AMR][1000 genomes] |
rs73854625 | 1.00[AMR][1000 genomes] |
rs73854626 | 1.00[AMR][1000 genomes] |
rs73854627 | 1.00[AMR][1000 genomes] |
rs73854628 | 1.00[AMR][1000 genomes] |
rs73856504 | 1.00[AMR][1000 genomes] |
rs73856505 | 1.00[AMR][1000 genomes] |
rs73856506 | 1.00[AMR][1000 genomes] |
rs73856507 | 1.00[AMR][1000 genomes] |
rs73856508 | 1.00[AMR][1000 genomes] |
rs73856509 | 1.00[AMR][1000 genomes] |
rs73856510 | 1.00[AMR][1000 genomes] |
rs73856517 | 1.00[AMR][1000 genomes] |
rs73856518 | 1.00[AMR][1000 genomes] |
rs73856520 | 1.00[AMR][1000 genomes] |
rs73856521 | 1.00[AMR][1000 genomes] |
rs73856522 | 1.00[AMR][1000 genomes] |
rs73856523 | 1.00[AMR][1000 genomes] |
rs73856524 | 1.00[AMR][1000 genomes] |
rs73856525 | 1.00[AMR][1000 genomes] |
rs73856527 | 1.00[AMR][1000 genomes] |
rs73856528 | 1.00[AMR][1000 genomes] |
rs73856530 | 1.00[AMR][1000 genomes] |
rs73856532 | 1.00[AMR][1000 genomes] |
rs73856533 | 1.00[AMR][1000 genomes] |
rs73856534 | 1.00[AMR][1000 genomes] |
rs73856536 | 1.00[AMR][1000 genomes] |
rs73856538 | 1.00[AMR][1000 genomes] |
rs73856540 | 1.00[AMR][1000 genomes] |
rs73856542 | 1.00[AMR][1000 genomes] |
rs73856546 | 1.00[AMR][1000 genomes] |
rs73856547 | 1.00[AMR][1000 genomes] |
rs73856548 | 1.00[AMR][1000 genomes] |
rs73856550 | 1.00[AMR][1000 genomes] |
rs73856553 | 1.00[AMR][1000 genomes] |
rs73856569 | 1.00[AMR][1000 genomes] |
rs73856574 | 1.00[AMR][1000 genomes] |
rs73857409 | 1.00[AMR][1000 genomes] |
rs73857410 | 1.00[AMR][1000 genomes] |
rs73857411 | 1.00[AMR][1000 genomes] |
rs73857413 | 1.00[AMR][1000 genomes] |
rs73857414 | 1.00[AMR][1000 genomes] |
rs73857415 | 1.00[AMR][1000 genomes] |
rs7432818 | 1.00[AMR][1000 genomes] |
rs7632428 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869347 | chr3:97742604-98051633 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 27 gene(s) | inside rSNPs | diseases |
2 | nsv877209 | chr3:97806616-98049409 | Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
3 | nsv963576 | chr3:97825434-98041343 | Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
4 | nsv1004820 | chr3:97852875-98169488 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
5 | nsv834773 | chr3:97855362-98043888 | Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
6 | nsv1000834 | chr3:97859880-98095473 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
7 | nsv877210 | chr3:97866177-97992964 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
8 | nsv432462 | chr3:97918267-98001710 | Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
9 | nsv877212 | chr3:97931105-98033400 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
10 | esv1842860 | chr3:97934241-98075543 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
11 | nsv1004762 | chr3:97935701-98000227 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
12 | nsv1008569 | chr3:97937168-97983117 | Enhancers Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
13 | nsv1009918 | chr3:97946030-98155450 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
14 | nsv965340 | chr3:97957002-97980365 | Weak transcription Enhancers | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
15 | esv3444875 | chr3:97957818-97983549 | Enhancers Weak transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
16 | nsv877213 | chr3:97973670-97992964 | Enhancers ZNF genes & repeats Weak transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
17 | esv3399236 | chr3:97977397-97988329 | Inactive region | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |