Variant report
Variant | rs73283734 |
---|---|
Chromosome Location | chr12:42653682-42653683 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr12:42652103..42654567-chr12:42656993..42659814,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11118 | 1.00[EUR][1000 genomes] |
rs11829039 | 1.00[EUR][1000 genomes] |
rs11829542 | 1.00[EUR][1000 genomes] |
rs11830248 | 1.00[EUR][1000 genomes] |
rs11830386 | 1.00[EUR][1000 genomes] |
rs11831464 | 1.00[EUR][1000 genomes] |
rs11832196 | 1.00[EUR][1000 genomes] |
rs11832840 | 1.00[EUR][1000 genomes] |
rs11833011 | 1.00[EUR][1000 genomes] |
rs11833109 | 1.00[EUR][1000 genomes] |
rs11833381 | 1.00[EUR][1000 genomes] |
rs11834665 | 1.00[EUR][1000 genomes] |
rs11837839 | 1.00[EUR][1000 genomes] |
rs1234103 | 1.00[EUR][1000 genomes] |
rs1626596 | 1.00[EUR][1000 genomes] |
rs1628339 | 1.00[EUR][1000 genomes] |
rs1683199 | 1.00[EUR][1000 genomes] |
rs1683203 | 1.00[EUR][1000 genomes] |
rs1688846 | 1.00[EUR][1000 genomes] |
rs1688876 | 1.00[EUR][1000 genomes] |
rs17091023 | 1.00[EUR][1000 genomes] |
rs1873684 | 1.00[EUR][1000 genomes] |
rs2406968 | 1.00[EUR][1000 genomes] |
rs2639131 | 1.00[EUR][1000 genomes] |
rs57435495 | 0.95[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs57647260 | 1.00[EUR][1000 genomes] |
rs57955254 | 1.00[EUR][1000 genomes] |
rs58229270 | 1.00[EUR][1000 genomes] |
rs58676357 | 1.00[EUR][1000 genomes] |
rs59190545 | 1.00[EUR][1000 genomes] |
rs60314019 | 1.00[EUR][1000 genomes] |
rs61067658 | 1.00[EUR][1000 genomes] |
rs7299386 | 1.00[EUR][1000 genomes] |
rs7305651 | 1.00[EUR][1000 genomes] |
rs73270269 | 1.00[EUR][1000 genomes] |
rs73270275 | 1.00[EUR][1000 genomes] |
rs73270279 | 1.00[EUR][1000 genomes] |
rs73270293 | 1.00[EUR][1000 genomes] |
rs73272004 | 1.00[EUR][1000 genomes] |
rs73272008 | 1.00[EUR][1000 genomes] |
rs73272013 | 0.81[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73272046 | 1.00[EUR][1000 genomes] |
rs73272047 | 1.00[EUR][1000 genomes] |
rs73272050 | 1.00[EUR][1000 genomes] |
rs73272072 | 1.00[EUR][1000 genomes] |
rs73272073 | 1.00[EUR][1000 genomes] |
rs73272080 | 1.00[EUR][1000 genomes] |
rs73272091 | 1.00[EUR][1000 genomes] |
rs73272101 | 1.00[EUR][1000 genomes] |
rs73273911 | 1.00[EUR][1000 genomes] |
rs73273932 | 1.00[EUR][1000 genomes] |
rs73281814 | 0.95[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73281820 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73281838 | 1.00[EUR][1000 genomes] |
rs73281851 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73281860 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73281880 | 1.00[EUR][1000 genomes] |
rs73281886 | 1.00[EUR][1000 genomes] |
rs73281894 | 1.00[EUR][1000 genomes] |
rs73283707 | 1.00[EUR][1000 genomes] |
rs73283759 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73283792 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73283799 | 1.00[EUR][1000 genomes] |
rs73285617 | 1.00[EUR][1000 genomes] |
rs73285619 | 1.00[EUR][1000 genomes] |
rs73285621 | 1.00[EUR][1000 genomes] |
rs73285631 | 0.90[AFR][1000 genomes] |
rs73285641 | 1.00[EUR][1000 genomes] |
rs73285662 | 1.00[EUR][1000 genomes] |
rs73285670 | 1.00[EUR][1000 genomes] |
rs7970895 | 1.00[EUR][1000 genomes] |
rs824690 | 1.00[EUR][1000 genomes] |
rs824696 | 1.00[EUR][1000 genomes] |
rs824715 | 1.00[EUR][1000 genomes] |
rs824719 | 1.00[EUR][1000 genomes] |
rs824720 | 1.00[EUR][1000 genomes] |
rs824721 | 1.00[EUR][1000 genomes] |
rs824723 | 1.00[EUR][1000 genomes] |
rs824725 | 1.00[EUR][1000 genomes] |
rs824727 | 1.00[EUR][1000 genomes] |
rs824729 | 1.00[EUR][1000 genomes] |
rs824731 | 1.00[EUR][1000 genomes] |
rs824732 | 1.00[EUR][1000 genomes] |
rs824733 | 1.00[EUR][1000 genomes] |
rs824735 | 1.00[EUR][1000 genomes] |
rs824737 | 1.00[EUR][1000 genomes] |
rs844045 | 1.00[EUR][1000 genomes] |
rs850964 | 1.00[EUR][1000 genomes] |
rs850965 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv430505 | chr12:42297931-42720773 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
2 | nsv826351 | chr12:42584218-42676281 | Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
3 | nsv826352 | chr12:42593124-42675255 | Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 18 gene(s) | inside rSNPs | diseases |
4 | esv3397788 | chr12:42636734-42665519 | Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
5 | nsv1048971 | chr12:42651976-42801204 | Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 12 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:42650200-42655600 | Weak transcription | Hela-S3 | cervix |