Variant report
Variant | rs4386952 |
---|---|
Chromosome Location | chr8:110102250-110102251 |
allele | A/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 | chr8:110096767..110098879-chr8:110100924..110103388,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000174417 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11785269 | 0.86[CHB][hapmap] |
rs12544197 | 0.83[CHB][hapmap] |
rs1548082 | 0.91[CHB][hapmap] |
rs1548083 | 0.91[CHB][hapmap];0.81[CHD][hapmap] |
rs16892486 | 0.86[CHB][hapmap];0.86[CHD][hapmap] |
rs16892496 | 0.86[CHB][hapmap];0.86[CHD][hapmap] |
rs2926198 | 0.91[CHB][hapmap] |
rs2980603 | 0.91[CHB][hapmap] |
rs2980618 | 0.85[CHB][hapmap];0.81[CHD][hapmap] |
rs3134105 | 0.82[CHB][hapmap] |
rs3925087 | 0.86[CHB][hapmap];0.86[CHD][hapmap] |
rs4130682 | 0.86[CHB][hapmap] |
rs4236801 | 0.86[CHB][hapmap];0.86[CHD][hapmap] |
rs4446710 | 0.86[CHB][hapmap];0.86[CHD][hapmap] |
rs4464939 | 0.86[CHB][hapmap] |
rs4546626 | 0.86[CHB][hapmap];0.86[CHD][hapmap] |
rs5772 | 0.82[JPT][hapmap] |
rs7823804 | 0.86[CHB][hapmap] |
rs7828207 | 0.86[CHB][hapmap] |
rs7830607 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7832552 | 0.86[CHB][hapmap];0.86[CHD][hapmap] |
rs7844643 | 0.86[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1022273 | chr8:110026712-110146600 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv539715 | chr8:110026712-110146600 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |