Variant report
Variant | rs2885471 |
---|---|
Chromosome Location | chr8:87669971-87669972 |
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 | chr8:87668814..87670322-chr8:87672192..87674304,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000205333 | Chromatin interaction |
ENSG00000233915 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1009574 | 0.87[CHB][hapmap] |
rs10107915 | 0.81[JPT][hapmap] |
rs11787263 | 0.81[CHB][hapmap] |
rs1219096 | 0.86[JPT][hapmap] |
rs12675140 | 0.86[JPT][hapmap] |
rs13268738 | 0.81[AMR][1000 genomes] |
rs13278423 | 0.81[JPT][hapmap] |
rs1348143 | 0.82[CHB][hapmap] |
rs1372170 | 0.86[JPT][hapmap] |
rs1441238 | 0.86[JPT][hapmap] |
rs1596027 | 0.86[JPT][hapmap] |
rs16916907 | 0.80[JPT][hapmap] |
rs2013536 | 0.90[CHB][hapmap];0.95[JPT][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs315973 | 0.87[JPT][hapmap] |
rs315976 | 0.86[JPT][hapmap] |
rs3779799 | 0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs4960985 | 0.90[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs4961212 | 0.81[CHB][hapmap] |
rs7014125 | 0.86[JPT][hapmap] |
rs7814749 | 0.86[JPT][hapmap] |
rs7842410 | 0.86[CHB][hapmap];0.90[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1023510 | chr8:87429001-87874948 | Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 31 gene(s) | inside rSNPs | diseases |
2 | nsv971682 | chr8:87669499-87671270 | Enhancers Weak transcription | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:87669400-87672000 | Enhancers | Pancreas | Pancrea |
2 | chr8:87669600-87670800 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |