Variant report
Variant | rs271257 |
---|---|
Chromosome Location | chr5:53167408-53167409 |
allele | A/G |
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:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr5:53029076..53030387-chr5:53166234..53167555,10 | MCF-7 | breast: | |
2 | chr5:53065681..53068308-chr5:53166800..53168407,2 | MCF-7 | breast: | |
3 | chr5:53029523..53030741-chr5:53166540..53167569,3 | MCF-7 | breast: | |
4 | chr5:52774000..52774674-chr5:53166806..53167591,2 | MCF-7 | breast: | |
5 | chr5:52778566..52779397-chr5:53166578..53167566,3 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs175248 | 1.00[EUR][1000 genomes] |
rs1979646 | 1.00[EUR][1000 genomes] |
rs1979647 | 1.00[EUR][1000 genomes] |
rs1981842 | 1.00[EUR][1000 genomes] |
rs199609 | 0.80[AFR][1000 genomes];0.88[ASN][1000 genomes] |
rs2042313 | 1.00[EUR][1000 genomes] |
rs271207 | 1.00[EUR][1000 genomes] |
rs271208 | 1.00[EUR][1000 genomes] |
rs271243 | 0.81[JPT][hapmap];1.00[EUR][1000 genomes] |
rs271245 | 1.00[EUR][1000 genomes] |
rs271250 | 0.82[CHB][hapmap];0.95[JPT][hapmap];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs271259 | 0.89[ASN][1000 genomes] |
rs271261 | 0.88[AFR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs37539 | 1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs37540 | 1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs3776740 | 1.00[EUR][1000 genomes] |
rs3797287 | 1.00[EUR][1000 genomes] |
rs3797290 | 1.00[EUR][1000 genomes] |
rs40211 | 0.86[CHB][hapmap];0.95[JPT][hapmap];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs40212 | 1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs6450173 | 1.00[EUR][1000 genomes] |
rs7733347 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2752745 | chr5:52422063-53343529 | Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
2 | nsv1032632 | chr5:52667145-53655624 | Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 29 gene(s) | inside rSNPs | diseases |
3 | nsv1032504 | chr5:52908394-53398435 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 13 gene(s) | inside rSNPs | diseases |
4 | nsv537763 | chr5:52908394-53398435 | Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 13 gene(s) | inside rSNPs | diseases |
5 | nsv830298 | chr5:52973912-53193398 | Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 5 gene(s) | inside rSNPs | diseases |
6 | nsv533778 | chr5:53092696-53284566 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
7 | nsv1019194 | chr5:53104869-53178957 | Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:53166400-53175400 | Weak transcription | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
2 | chr5:53166800-53176800 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
3 | chr5:53167000-53170400 | Weak transcription | Osteobl | bone |