Variant report
Variant | rs1447131 |
---|---|
Chromosome Location | chr6:55751496-55751497 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:5)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:5 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr6:55313713..55314676-chr6:55750196..55751674,4 | MCF-7 | breast: | |
2 | chr6:55314098..55314636-chr6:55750998..55751586,2 | MCF-7 | breast: | |
3 | chr6:55310131..55310914-chr6:55750826..55751625,3 | MCF-7 | breast: | |
4 | chr6:55751118..55751828-chr6:55818205..55818779,2 | MCF-7 | breast: | |
5 | chr6:55481775..55483073-chr6:55750730..55751770,11 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs12198217 | 0.85[EUR][1000 genomes] |
rs1374550 | 0.86[CHB][hapmap];1.00[JPT][hapmap] |
rs1447128 | 0.88[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs1447132 | 0.82[AFR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1562408 | 0.85[EUR][1000 genomes] |
rs1838946 | 0.88[EUR][1000 genomes] |
rs1868031 | 0.81[ASN][1000 genomes] |
rs2021803 | 0.89[CHD][hapmap];1.00[JPT][hapmap] |
rs2028956 | 0.88[EUR][1000 genomes] |
rs2044543 | 0.85[EUR][1000 genomes] |
rs2056424 | 0.85[EUR][1000 genomes] |
rs3734444 | 0.85[CHD][hapmap];1.00[JPT][hapmap] |
rs3798819 | 0.81[JPT][hapmap] |
rs3807016 | 0.89[CHD][hapmap];1.00[JPT][hapmap] |
rs4715567 | 1.00[JPT][hapmap] |
rs4715570 | 0.85[EUR][1000 genomes] |
rs4715571 | 0.85[CEU][hapmap] |
rs6459112 | 0.88[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs6459113 | 0.85[EUR][1000 genomes] |
rs6912214 | 0.89[CHD][hapmap];1.00[JPT][hapmap] |
rs6925961 | 0.85[EUR][1000 genomes] |
rs6926331 | 0.81[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs6932412 | 0.88[EUR][1000 genomes] |
rs72870626 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7752119 | 0.85[EUR][1000 genomes] |
rs7755393 | 0.80[EUR][1000 genomes] |
rs7758580 | 0.81[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9296807 | 0.81[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9296809 | 0.85[EUR][1000 genomes] |
rs9296810 | 0.85[EUR][1000 genomes] |
rs9464298 | 1.00[JPT][hapmap] |
rs9464303 | 0.85[EUR][1000 genomes] |
rs9475467 | 0.85[EUR][1000 genomes] |
rs9475469 | 0.85[EUR][1000 genomes] |
rs9475471 | 0.85[EUR][1000 genomes] |
rs978930 | 0.89[CHD][hapmap];1.00[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1034037 | chr6:55222409-56069600 | Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
2 | esv2752670 | chr6:55614978-55781605 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
3 | nsv1032684 | chr6:55680473-55766876 | Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
4 | nsv1024174 | chr6:55713889-55829936 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
5 | nsv1029301 | chr6:55713889-55834480 | Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:55749600-55751600 | Enhancers | Fetal Lung | lung |
2 | chr6:55751200-55752200 | Enhancers | HepG2 | liver |
3 | chr6:55751400-55751600 | Enhancers | Hela-S3 | cervix |
4 | chr6:55751400-55751800 | Enhancers | A549 | lung |