Variant report
Variant | rs7637567 |
---|---|
Chromosome Location | chr3:151190481-151190482 |
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 | chr3:151189546..151191159-chr3:151195430..151197288,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10935854 | 0.85[CEU][hapmap];0.82[CHD][hapmap];0.83[JPT][hapmap] |
rs12485986 | 0.93[CEU][hapmap];0.90[CHB][hapmap];0.92[JPT][hapmap];0.97[ASN][1000 genomes] |
rs4234328 | 0.97[ASN][1000 genomes] |
rs4234329 | 0.97[ASN][1000 genomes] |
rs4266168 | 0.97[ASN][1000 genomes] |
rs4339091 | 0.97[ASN][1000 genomes] |
rs4532110 | 0.97[ASN][1000 genomes] |
rs4541381 | 0.93[CEU][hapmap];0.90[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap] |
rs4550807 | 0.97[ASN][1000 genomes] |
rs4596123 | 0.93[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap] |
rs4605516 | 0.97[ASN][1000 genomes] |
rs4679835 | 0.93[CEU][hapmap];0.90[CHB][hapmap];0.91[JPT][hapmap];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4679847 | 0.97[ASN][1000 genomes] |
rs4680484 | 0.97[ASN][1000 genomes] |
rs6440749 | 0.85[CEU][hapmap];0.83[JPT][hapmap] |
rs6440757 | 0.97[ASN][1000 genomes] |
rs6773513 | 0.85[CEU][hapmap];0.82[JPT][hapmap] |
rs6786901 | 0.97[ASN][1000 genomes] |
rs7615314 | 0.93[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes] |
rs7622835 | 0.97[ASN][1000 genomes] |
rs7629176 | 0.97[ASN][1000 genomes] |
rs7637276 | 0.94[ASN][1000 genomes] |
rs9289848 | 0.97[ASN][1000 genomes] |
rs9811627 | 0.97[ASN][1000 genomes] |
rs9816549 | 0.97[ASN][1000 genomes] |
rs9821181 | 0.94[ASN][1000 genomes] |
rs9825219 | 0.97[ASN][1000 genomes] |
rs9829893 | 0.97[ASN][1000 genomes] |
rs9877416 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs9880648 | 0.97[ASN][1000 genomes] |
rs9882955 | 0.97[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv829757 | chr3:151044880-151226442 | Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
2 | nsv1000355 | chr3:151108859-151243835 | Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 5 gene(s) | inside rSNPs | diseases |
3 | nsv995048 | chr3:151114074-151560019 | Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 12 gene(s) | inside rSNPs | diseases |
4 | nsv877649 | chr3:151147968-151236562 | Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 3 gene(s) | inside rSNPs | diseases |
5 | nsv877650 | chr3:151174010-151314449 | Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:151179200-151194200 | Weak transcription | Ovary | ovary |
2 | chr3:151188600-151194000 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |