Variant report
Variant | rs11887536 |
---|---|
Chromosome Location | chr2:99507286-99507287 |
allele | A/G |
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 | chr2:99505531..99508517-chr2:99513277..99515165,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10169003 | 0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10172158 | 0.91[EUR][1000 genomes] |
rs10181972 | 0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs10188156 | 0.88[EUR][1000 genomes] |
rs11123755 | 0.91[EUR][1000 genomes] |
rs11123756 | 0.84[AFR][1000 genomes] |
rs11893888 | 0.86[EUR][1000 genomes] |
rs12468024 | 0.91[EUR][1000 genomes] |
rs12474283 | 0.80[EUR][1000 genomes] |
rs12712035 | 0.87[EUR][1000 genomes] |
rs12712036 | 0.84[EUR][1000 genomes] |
rs12712038 | 0.91[EUR][1000 genomes] |
rs12712039 | 0.85[AFR][1000 genomes];0.91[EUR][1000 genomes] |
rs12992214 | 0.80[ASN][1000 genomes] |
rs13004923 | 0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs1356424 | 0.80[EUR][1000 genomes] |
rs1581250 | 0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs1581251 | 0.91[EUR][1000 genomes] |
rs1878585 | 0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs1949424 | 0.84[ASN][1000 genomes] |
rs1962029 | 0.82[AFR][1000 genomes] |
rs1983352 | 0.87[EUR][1000 genomes] |
rs2280256 | 0.83[EUR][1000 genomes] |
rs4263159 | 0.88[EUR][1000 genomes] |
rs4553869 | 0.84[AFR][1000 genomes] |
rs4850888 | 0.87[EUR][1000 genomes] |
rs4850889 | 0.80[EUR][1000 genomes] |
rs4851162 | 0.88[EUR][1000 genomes] |
rs4851163 | 0.88[EUR][1000 genomes] |
rs4851167 | 0.91[EUR][1000 genomes] |
rs4851170 | 0.91[EUR][1000 genomes] |
rs4851171 | 0.91[EUR][1000 genomes] |
rs4851173 | 0.80[EUR][1000 genomes] |
rs4851177 | 0.81[EUR][1000 genomes] |
rs6419564 | 0.81[EUR][1000 genomes] |
rs6542838 | 0.88[EUR][1000 genomes] |
rs6542839 | 0.84[EUR][1000 genomes] |
rs6542841 | 0.84[AFR][1000 genomes] |
rs6542843 | 0.81[EUR][1000 genomes] |
rs6704682 | 0.84[AFR][1000 genomes] |
rs6711022 | 0.83[EUR][1000 genomes] |
rs6713991 | 0.88[EUR][1000 genomes] |
rs6714243 | 0.91[EUR][1000 genomes] |
rs6717372 | 0.91[EUR][1000 genomes] |
rs6719634 | 0.84[EUR][1000 genomes] |
rs6726156 | 0.84[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs6739097 | 0.81[ASN][1000 genomes] |
rs6739176 | 0.81[EUR][1000 genomes] |
rs6739503 | 0.80[EUR][1000 genomes] |
rs6752025 | 0.86[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs7565510 | 0.83[AFR][1000 genomes] |
rs7579189 | 0.88[EUR][1000 genomes] |
rs7593332 | 0.85[ASN][1000 genomes] |
rs7608889 | 0.91[EUR][1000 genomes] |
rs883773 | 0.84[AFR][1000 genomes] |
rs925887 | 0.84[EUR][1000 genomes] |
rs981601 | 0.88[EUR][1000 genomes] |
rs981602 | 0.87[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1011278 | chr2:99280928-99638376 | Weak transcription Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
2 | nsv535835 | chr2:99280928-99638376 | Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
3 | nsv582518 | chr2:99498774-99546355 | Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:99500000-99517000 | Weak transcription | Gastric | stomach |