Variant report
Variant | rs4754744 |
---|---|
Chromosome Location | chr11:101128447-101128448 |
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:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr11:100999307..101001202-chr11:101126691..101128558,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000082175 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10791449 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs1783747 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[EUR][1000 genomes] |
rs1942839 | 0.95[AMR][1000 genomes] |
rs1942840 | 0.80[AFR][1000 genomes] |
rs1943758 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2156520 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs4121760 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs4144343 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs4237600 | 1.00[AMR][1000 genomes] |
rs4282959 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs4335511 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs4351785 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs4754008 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs528237 | 0.81[EUR][1000 genomes] |
rs528399 | 0.90[AMR][1000 genomes] |
rs538458 | 0.90[AMR][1000 genomes] |
rs572915 | 0.81[AMR][1000 genomes] |
rs606386 | 0.85[AMR][1000 genomes] |
rs607699 | 0.85[AMR][1000 genomes] |
rs6590841 | 0.90[AMR][1000 genomes] |
rs6590842 | 1.00[AMR][1000 genomes] |
rs7102599 | 0.86[AMR][1000 genomes] |
rs7104105 | 0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs7110399 | 1.00[AMR][1000 genomes] |
rs7119902 | 0.90[AMR][1000 genomes] |
rs7128630 | 0.81[AFR][1000 genomes];0.95[AMR][1000 genomes] |
rs7342177 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7342182 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7932597 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7942104 | 0.90[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs877627 | 0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs948749 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs948891 | 0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs948892 | 0.95[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv556131 | chr11:100985777-101480017 | Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv530644 | chr11:101010088-101486038 | Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
3 | esv2753322 | chr11:101052790-101311790 | Flanking Bivalent TSS/Enh Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv832247 | chr11:101123483-101298787 | Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:101126200-101130400 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
2 | chr11:101126400-101169400 | Weak transcription | Ovary | ovary |