Variant report
Variant | rs11887304 |
---|---|
Chromosome Location | chr2:142243843-142243844 |
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 | chr2:142241833..142244486-chr2:142265674..142268047,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10496881 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs11898305 | 0.82[JPT][hapmap] |
rs1483144 | 0.86[JPT][hapmap] |
rs16846183 | 1.00[ASN][1000 genomes] |
rs16846216 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs16846224 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs16846251 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs16846272 | 1.00[ASN][1000 genomes] |
rs16846274 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs16846416 | 1.00[JPT][hapmap] |
rs16846509 | 1.00[JPT][hapmap] |
rs16846539 | 1.00[JPT][hapmap] |
rs16855055 | 1.00[JPT][hapmap];0.90[ASN][1000 genomes] |
rs1905291 | 0.85[JPT][hapmap] |
rs41396347 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs4271711 | 0.97[ASN][1000 genomes] |
rs4491668 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4547471 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4560051 | 0.85[JPT][hapmap] |
rs4575660 | 0.85[JPT][hapmap] |
rs4954914 | 0.86[JPT][hapmap] |
rs62167901 | 0.90[ASN][1000 genomes] |
rs62167934 | 0.85[ASN][1000 genomes] |
rs62167935 | 0.85[ASN][1000 genomes] |
rs6429898 | 0.86[JPT][hapmap] |
rs6708984 | 0.85[JPT][hapmap] |
rs6717169 | 0.85[JPT][hapmap] |
rs6749551 | 0.86[JPT][hapmap] |
rs72849629 | 1.00[ASN][1000 genomes] |
rs72849660 | 1.00[ASN][1000 genomes] |
rs72849666 | 1.00[ASN][1000 genomes] |
rs72851323 | 1.00[ASN][1000 genomes] |
rs72851325 | 1.00[ASN][1000 genomes] |
rs72851386 | 0.90[ASN][1000 genomes] |
rs72852436 | 0.90[ASN][1000 genomes] |
rs72852464 | 0.90[ASN][1000 genomes] |
rs7557886 | 1.00[ASN][1000 genomes] |
rs7576810 | 0.85[ASN][1000 genomes] |
rs9287319 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv817518 | chr2:141714174-142287302 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv583203 | chr2:142055133-142378975 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | esv2759095 | chr2:142071391-142245947 | Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv875234 | chr2:142156180-142254119 | Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
5 | esv2756949 | chr2:142196123-142245947 | Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
6 | nsv875240 | chr2:142199421-142347455 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer | Chromatin interactive region | 2 gene(s) | inside rSNPs | n/a |
7 | nsv875243 | chr2:142219033-142259592 | Enhancers Weak transcription Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
8 | nsv459607 | chr2:142226768-142263400 | Enhancers Weak transcription Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
9 | nsv583207 | chr2:142226768-142263400 | Enhancers Weak transcription Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:142239400-142256400 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |